

Hero image 0 of Code of Federal Regulations Title 21, Volume 8, April 1, 2015 (Paperback), 0 of 1
Code of Federal Regulations Title 21, Volume 8, April 1, 2015 (Paperback)
(No ratings yet)
Key item features
21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anesthesiology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, human tissue intended for transplantation, and more.
Health care device manufacturers, hospital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and health care policy advocates may be interested in this volume.
Code of Federal Regulations Title 21, Volume 8, April 1, 2015
Containing parts Parts 800 to 1299
Part 800; GENERAL
Part 801; LABELING
Part 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Part 810; MEDICAL DEVICE RECALL AUTHORITY
Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS
Part 813; Reserved
Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES
Part 820; QUALITY SYSTEM REGULATION
Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS
Part 822; POSTMARKET SURVEILLANCE
Part 830; UNIQUE DEVICE IDENTIFICATION
Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES
Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
Part 864; HEMATOLOGY AND PATHOLOGY DEVICES
Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES
Part 868; ANESTHESIOLOGY DEVICES
Part 870; CARDIOVASCULAR DEVICES
Part 872; DENTAL DEVICES
Part 874; EAR, NOSE, AND THROAT DEVICES
Part 876; GASTROENTEROLOGY-UROLOGY DEVICES
Part 878; GENERAL AND PLASTIC SURGERY DEVICES
Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES
Part 882; NEUROLOGICAL DEVICES
Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES
Part 886; OPHTHALMIC DEVICES
Part 888; ORTHOPEDIC DEVICES
Part 890; PHYSICAL MEDICINE DEVICES
Part 892; RADIOLOGY DEVICES
Part 895; BANNED DEVICES
Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
Part 900; MAMMOGRAPHY
Part 1000; GENERAL
Part 1002; RECORDS AND REPORTS
Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS
Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
Part 1140; CIGARETTES AND SMOKELESS TOBACCO
Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS
Part 1150; USER FEES
Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
Part 1240; CONTROL OF COMMUNICABLE DISEASES
Part 1250; INTERSTATE CONVEYANCE SANITATION
Parts 1251-1269; Reserved
Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION
Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
Parts 1272-1299; Reserved
Health care device manufacturers, hospital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and health care policy advocates may be interested in this volume.
Code of Federal Regulations Title 21, Volume 8, April 1, 2015
Containing parts Parts 800 to 1299
Part 800; GENERAL
Part 801; LABELING
Part 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Part 810; MEDICAL DEVICE RECALL AUTHORITY
Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS
Part 813; Reserved
Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES
Part 820; QUALITY SYSTEM REGULATION
Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS
Part 822; POSTMARKET SURVEILLANCE
Part 830; UNIQUE DEVICE IDENTIFICATION
Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES
Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
Part 864; HEMATOLOGY AND PATHOLOGY DEVICES
Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES
Part 868; ANESTHESIOLOGY DEVICES
Part 870; CARDIOVASCULAR DEVICES
Part 872; DENTAL DEVICES
Part 874; EAR, NOSE, AND THROAT DEVICES
Part 876; GASTROENTEROLOGY-UROLOGY DEVICES
Part 878; GENERAL AND PLASTIC SURGERY DEVICES
Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES
Part 882; NEUROLOGICAL DEVICES
Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES
Part 886; OPHTHALMIC DEVICES
Part 888; ORTHOPEDIC DEVICES
Part 890; PHYSICAL MEDICINE DEVICES
Part 892; RADIOLOGY DEVICES
Part 895; BANNED DEVICES
Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
Part 900; MAMMOGRAPHY
Part 1000; GENERAL
Part 1002; RECORDS AND REPORTS
Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS
Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
Part 1140; CIGARETTES AND SMOKELESS TOBACCO
Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS
Part 1150; USER FEES
Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
Part 1240; CONTROL OF COMMUNICABLE DISEASES
Part 1250; INTERSTATE CONVEYANCE SANITATION
Parts 1251-1269; Reserved
Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION
Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
Parts 1272-1299; Reserved
Specs
- Book formatPaperback
- Fiction/nonfictionNon-Fiction
- Pub dateApril 1, 2015
- Pages862
- SubgenreLaw
- EditionStandard Edition
Current price is USD$64.95
Price when purchased online
- Free shipping
Free 90-day returns
How do you want your item?
Try 30 days of Free Shipping with Walmart+! Choose plan at checkout.
Columbus, 43215
Arrives by Thu, Apr 9
Sold and shipped by Walmart.com
Free 90-day returns
This item is gift eligible
Get free delivery, shipping and more*
*Restrictions apply Try Walmart+ now
About this item
Product details
21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anesthesiology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, human tissue intended for transplantation, and more.
Health care device manufacturers, hospital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and health care policy advocates may be interested in this volume.
Code of Federal Regulations Title 21, Volume 8, April 1, 2015
Containing parts Parts 800 to 1299
Part 800; GENERAL
Part 801; LABELING
Part 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Part 810; MEDICAL DEVICE RECALL AUTHORITY
Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS
Part 813; Reserved
Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES
Part 820; QUALITY SYSTEM REGULATION
Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS
Part 822; POSTMARKET SURVEILLANCE
Part 830; UNIQUE DEVICE IDENTIFICATION
Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES
Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
Part 864; HEMATOLOGY AND PATHOLOGY DEVICES
Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES
Part 868; ANESTHESIOLOGY DEVICES
Part 870; CARDIOVASCULAR DEVICES
Part 872; DENTAL DEVICES
Part 874; EAR, NOSE, AND THROAT DEVICES
Part 876; GASTROENTEROLOGY-UROLOGY DEVICES
Part 878; GENERAL AND PLASTIC SURGERY DEVICES
Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES
Part 882; NEUROLOGICAL DEVICES
Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES
Part 886; OPHTHALMIC DEVICES
Part 888; ORTHOPEDIC DEVICES
Part 890; PHYSICAL MEDICINE DEVICES
Part 892; RADIOLOGY DEVICES
Part 895; BANNED DEVICES
Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
Part 900; MAMMOGRAPHY
Part 1000; GENERAL
Part 1002; RECORDS AND REPORTS
Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS
Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
Part 1140; CIGARETTES AND SMOKELESS TOBACCO
Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS
Part 1150; USER FEES
Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
Part 1240; CONTROL OF COMMUNICABLE DISEASES
Part 1250; INTERSTATE CONVEYANCE SANITATION
Parts 1251-1269; Reserved
Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION
Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
Parts 1272-1299; Reserved
Health care device manufacturers, hospital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and health care policy advocates may be interested in this volume.
Code of Federal Regulations Title 21, Volume 8, April 1, 2015
Containing parts Parts 800 to 1299
Part 800; GENERAL
Part 801; LABELING
Part 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Part 810; MEDICAL DEVICE RECALL AUTHORITY
Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS
Part 813; Reserved
Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES
Part 820; QUALITY SYSTEM REGULATION
Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS
Part 822; POSTMARKET SURVEILLANCE
Part 830; UNIQUE DEVICE IDENTIFICATION
Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES
Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
Part 864; HEMATOLOGY AND PATHOLOGY DEVICES
Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES
Part 868; ANESTHESIOLOGY DEVICES
Part 870; CARDIOVASCULAR DEVICES
Part 872; DENTAL DEVICES
Part 874; EAR, NOSE, AND THROAT DEVICES
Part 876; GASTROENTEROLOGY-UROLOGY DEVICES
Part 878; GENERAL AND PLASTIC SURGERY DEVICES
Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES
Part 882; NEUROLOGICAL DEVICES
Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES
Part 886; OPHTHALMIC DEVICES
Part 888; ORTHOPEDIC DEVICES
Part 890; PHYSICAL MEDICINE DEVICES
Part 892; RADIOLOGY DEVICES
Part 895; BANNED DEVICES
Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
Part 900; MAMMOGRAPHY
Part 1000; GENERAL
Part 1002; RECORDS AND REPORTS
Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS
Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
Part 1140; CIGARETTES AND SMOKELESS TOBACCO
Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS
Part 1150; USER FEES
Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
Part 1240; CONTROL OF COMMUNICABLE DISEASES
Part 1250; INTERSTATE CONVEYANCE SANITATION
Parts 1251-1269; Reserved
Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION
Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
Parts 1272-1299; Reserved
info:
We aim to show you accurate product information. Manufacturers, suppliers and others provide what you see here, and we have not verified it. Â
Specifications
Book format
Paperback
Fiction/nonfiction
Non-Fiction
Genre
Law/Administrative Law & Regulatory Practice, Law/Government - Federal
Pub date
April 1, 2015
Similar items you might like
Based on what customers bought
Code of Federal Regulations Title 20, Volume 1, April 1, 2015 (Paperback) $66.75
$6675current price $66.75Code of Federal Regulations Title 20, Volume 1, April 1, 2015 (Paperback)
Code of Federal Regulations Title 40, Volume 20, July 1, 2015 (Paperback) $78.57
$7857current price $78.57Code of Federal Regulations Title 40, Volume 20, July 1, 2015 (Paperback)
Code of Federal Regulations Title 46, Volume 9, October 1, 2015 (Paperback) $54.92
$5492current price $54.92Code of Federal Regulations Title 46, Volume 9, October 1, 2015 (Paperback)
Code of Federal Regulations Title 40, Volume 6, July 1, 2015 (Paperback) $66.75
$6675current price $66.75Code of Federal Regulations Title 40, Volume 6, July 1, 2015 (Paperback)
Code of Federal Regulations Title 47, Volume 4, October 1, 2015 (Paperback) $79.99
$7999current price $79.99Code of Federal Regulations Title 47, Volume 4, October 1, 2015 (Paperback)
Code of Federal Regulations Title 34, Volume 1, July 1, 2015 (Paperback) $66.75
$6675current price $66.75Code of Federal Regulations Title 34, Volume 1, July 1, 2015 (Paperback)
Code of Federal Regulations Title 26, Volume 19, April 1, 2015 (Paperback) $54.95
$5495current price $54.95Code of Federal Regulations Title 26, Volume 19, April 1, 2015 (Paperback)
Code of Federal Regulations Title 12, Volume 8, January 1, 2016 (Paperback) $68.95
$6895current price $68.95Code of Federal Regulations Title 12, Volume 8, January 1, 2016 (Paperback)
Code of Federal Regulations Title 37, Volume 1, July 1, 2015 (Paperback) $66.95
$6695current price $66.95Code of Federal Regulations Title 37, Volume 1, July 1, 2015 (Paperback)
Code of Federal Regulations Title 29, Volume 7, July 1, 2015 (Paperback) $54.92
$5492current price $54.92Code of Federal Regulations Title 29, Volume 7, July 1, 2015 (Paperback)
Code of Federal Regulations Title 27, Volume 1, April 1, 2015 (Paperback) $66.95
$6695current price $66.95Code of Federal Regulations Title 27, Volume 1, April 1, 2015 (Paperback)
Code of Federal Regulations Title 20, Volume 3, April 1, 2015 (Paperback) $66.75
$6675current price $66.75Code of Federal Regulations Title 20, Volume 3, April 1, 2015 (Paperback)
Code of Federal Regulations Title 7, Volume 3, January 1, 2016 (Paperback) $68.95
$6895current price $68.95Code of Federal Regulations Title 7, Volume 3, January 1, 2016 (Paperback)
Code of Federal Regulations Title 12, Volume 3, January 1, 2015 (Paperback) $69.95
$6995current price $69.95Code of Federal Regulations Title 12, Volume 3, January 1, 2015 (Paperback)
Code of Federal Regulations Title 24, Volume 2, April 1, 2015 (Paperback) $64.95
$6495current price $64.95Code of Federal Regulations Title 24, Volume 2, April 1, 2015 (Paperback)
Code of Federal Regulations Title 50, Volume 4, October 1, 2015 (Paperback) $66.95
$6695current price $66.95Code of Federal Regulations Title 50, Volume 4, October 1, 2015 (Paperback)
Code of Federal Regulations Title 12, Volume 3, January 1, 2016 (Paperback) $87.95
$8795current price $87.95Code of Federal Regulations Title 12, Volume 3, January 1, 2016 (Paperback)
Code of Federal Regulations Title 40, Volume 5, July 1, 2015 (Paperback) $66.75
$6675current price $66.75Code of Federal Regulations Title 40, Volume 5, July 1, 2015 (Paperback)
Code of Federal Regulations Title 24, Volume 4, April 1, 2015 (Paperback) $64.95
$6495current price $64.95Code of Federal Regulations Title 24, Volume 4, April 1, 2015 (Paperback)
Code of Federal Regulations Title 38, Volume 1, July 1, 2015 (Paperback) $78.57
$7857current price $78.57Code of Federal Regulations Title 38, Volume 1, July 1, 2015 (Paperback)
Customer ratings & reviews
0 ratings|0 reviews
This item does not have any reviews yet
