{"product_id":"code-of-federal-regulations-title-21-volume-8-april-1-2015-paperback","title":"Code of Federal Regulations Title 21, Volume 8, April 1, 2015 - Paperback","description":"\u003cdiv\u003e\u003cp style=\"text-align: right;\"\u003e\u003ca href=\"https:\/\/reportcopyrightinfringement.com\/\" target=\"_blank\" rel=\"nofollow\"\u003e\u003cb\u003eReport copyright infringement\u003c\/b\u003e\u003c\/a\u003e\u003c\/p\u003e\u003c\/div\u003e\u003cp\u003eby \u003cb\u003eOffice of the Federal Register\u003c\/b\u003e (Created by)\u003c\/p\u003e\u003cp\u003e21 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.\u003cbr\u003eHealth 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.\u003cbr\u003e\u003cbr\u003eCode of Federal Regulations Title 21, Volume 8, April 1, 2015\u003cbr\u003e\u003cbr\u003eContaining parts Parts 800 to 1299\u003cbr\u003e\u003cbr\u003ePart 800; GENERAL\u003cbr\u003ePart 801; LABELING\u003cbr\u003ePart 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)\u003cbr\u003ePart 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS\u003cbr\u003ePart 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES\u003cbr\u003ePart 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS\u003cbr\u003ePart 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE\u003cbr\u003ePart 810; MEDICAL DEVICE RECALL AUTHORITY\u003cbr\u003ePart 812; INVESTIGATIONAL DEVICE EXEMPTIONS\u003cbr\u003ePart 813; Reserved\u003cbr\u003ePart 814; PREMARKET APPROVAL OF MEDICAL DEVICES\u003cbr\u003ePart 820; QUALITY SYSTEM REGULATION\u003cbr\u003ePart 821; MEDICAL DEVICE TRACKING REQUIREMENTS\u003cbr\u003ePart 822; POSTMARKET SURVEILLANCE\u003cbr\u003ePart 830; UNIQUE DEVICE IDENTIFICATION\u003cbr\u003ePart 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES\u003cbr\u003ePart 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT\u003cbr\u003ePart 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES\u003cbr\u003ePart 864; HEMATOLOGY AND PATHOLOGY DEVICES\u003cbr\u003ePart 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES\u003cbr\u003ePart 868; ANESTHESIOLOGY DEVICES\u003cbr\u003ePart 870; CARDIOVASCULAR DEVICES\u003cbr\u003ePart 872; DENTAL DEVICES\u003cbr\u003ePart 874; EAR, NOSE, AND THROAT DEVICES\u003cbr\u003ePart 876; GASTROENTEROLOGY-UROLOGY DEVICES\u003cbr\u003ePart 878; GENERAL AND PLASTIC SURGERY DEVICES\u003cbr\u003ePart 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES\u003cbr\u003ePart 882; NEUROLOGICAL DEVICES\u003cbr\u003ePart 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES\u003cbr\u003ePart 886; OPHTHALMIC DEVICES\u003cbr\u003ePart 888; ORTHOPEDIC DEVICES\u003cbr\u003ePart 890; PHYSICAL MEDICINE DEVICES\u003cbr\u003ePart 892; RADIOLOGY DEVICES\u003cbr\u003ePart 895; BANNED DEVICES\u003cbr\u003ePart 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES\u003cbr\u003ePart 900; MAMMOGRAPHY\u003cbr\u003ePart 1000; GENERAL\u003cbr\u003ePart 1002; RECORDS AND REPORTS\u003cbr\u003ePart 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY\u003cbr\u003ePart 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS\u003cbr\u003ePart 1005; IMPORTATION OF ELECTRONIC PRODUCTS\u003cbr\u003ePart 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL\u003cbr\u003ePart 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS\u003cbr\u003ePart 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS\u003cbr\u003ePart 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS\u003cbr\u003ePart 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS\u003cbr\u003ePart 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS\u003cbr\u003ePart 1140; CIGARETTES AND SMOKELESS TOBACCO\u003cbr\u003ePart 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS\u003cbr\u003ePart 1150; USER FEES\u003cbr\u003ePart 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT\u003cbr\u003ePart 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT\u003cbr\u003ePart 1240; CONTROL OF COMMUNICABLE DISEASES\u003cbr\u003ePart 1250; INTERSTATE CONVEYANCE SANITATION\u003cbr\u003eParts 1251-1269; Reserved\u003cbr\u003ePart 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION\u003cbr\u003ePart 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS\u003cbr\u003eParts 1272-1299; Reserved\u003c\/p\u003e\n            \u003cdiv\u003e\n\u003cstrong\u003eNumber of Pages:\u003c\/strong\u003e 862\u003c\/div\u003e\n            \u003cdiv\u003e\n\u003cstrong\u003eDimensions:\u003c\/strong\u003e 1.71 x 9.21 x 6.14 IN\u003c\/div\u003e\n            \u003cdiv\u003e\n\u003cstrong\u003ePublication Date:\u003c\/strong\u003e March 01, 2016\u003c\/div\u003e\n            ","brand":"BooksCloud","offers":[{"title":"Default Title","offer_id":50731475861810,"sku":"9781354240236","price":123.91,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0961\/1608\/0946\/files\/IyI1B4cdw29781354240236.webp?v=1765770939","url":"https:\/\/deskinlawfirm.com\/products\/code-of-federal-regulations-title-21-volume-8-april-1-2015-paperback","provider":"DLF Bookstore","version":"1.0","type":"link"}