{"product_id":"cfr-21-parts-800-to-1299-food-and-drugs-april-01-2017-volume-8-of-9-9781298709196","title":"CFR 21, Parts 800 to 1299, Food and Drugs, April 01, 2017 (Volume 8 of 9)","description":"\u003cp\u003eCode of Federal Regulations Title 21, Volume 8, April 1, 2017 contains regulations governing Food and Drugs and may also be referenced as: \u003c\/p\u003e\u003cp\u003e- Code of Federal Regulations Title 21, Volume 8, April 1, 2017\u003cbr\u003e- CFR Title 21\u003cbr\u003e- CFR 21, Food and Drugs\u003cbr\u003e- CFR 21, Parts 800 to 1299, Food and Drugs\u003cbr\u003e\u003c\/p\u003e\u003cp\u003eThis volume contains Parts 800 to 1299: \u003c\/p\u003e\u003cp\u003e- Part 800; GENERAL\u003cbr\u003e- Part 801; LABELING\u003cbr\u003e- Part 803; MEDICAL DEVICE REPORTING\u003cbr\u003e- Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS\u003cbr\u003e- Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES\u003cbr\u003e- Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS\u003cbr\u003e- Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE\u003cbr\u003e- Part 810; MEDICAL DEVICE RECALL AUTHORITY\u003cbr\u003e- Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS\u003cbr\u003e- Part 813; Reserved\u003cbr\u003e- Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES\u003cbr\u003e- Part 820; QUALITY SYSTEM REGULATION\u003cbr\u003e- Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS\u003cbr\u003e- Part 822; POSTMARKET SURVEILLANCE\u003cbr\u003e- Part 830; UNIQUE DEVICE IDENTIFICATION\u003cbr\u003e- Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES\u003cbr\u003e- Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT\u003cbr\u003e- Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES\u003cbr\u003e- Part 864; HEMATOLOGY AND PATHOLOGY DEVICES\u003cbr\u003e- Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES\u003cbr\u003e- Part 868; ANESTHESIOLOGY DEVICES\u003cbr\u003e- Part 870; CARDIOVASCULAR DEVICES\u003cbr\u003e- Part 872; DENTAL DEVICES\u003cbr\u003e- Part 874; EAR, NOSE, AND THROAT DEVICES\u003cbr\u003e- Part 876; GASTROENTEROLOGY-UROLOGY DEVICES\u003cbr\u003e- Part 878; GENERAL AND PLASTIC SURGERY DEVICES\u003cbr\u003e- Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES\u003cbr\u003e- Part 882; NEUROLOGICAL DEVICES\u003cbr\u003e- Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES\u003cbr\u003e- Part 886; OPHTHALMIC DEVICES\u003cbr\u003e- Part 888; ORTHOPEDIC DEVICES\u003cbr\u003e- Part 890; PHYSICAL MEDICINE DEVICES\u003cbr\u003e- Part 892; RADIOLOGY DEVICES\u003cbr\u003e- Part 895; BANNED DEVICES\u003cbr\u003e- Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES\u003cbr\u003e- Part 900; MAMMOGRAPHY\u003cbr\u003e- Part 1000; GENERAL\u003cbr\u003e- Part 1002; RECORDS AND REPORTS\u003cbr\u003e- Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY\u003cbr\u003e- Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS\u003cbr\u003e- Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS\u003cbr\u003e- Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL\u003cbr\u003e- Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS\u003cbr\u003e- Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS\u003cbr\u003e- Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS\u003cbr\u003e- Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS\u003cbr\u003e- Part 1100; TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY\u003cbr\u003e- Part 1105; GENERAL\u003cbr\u003e- Part 1105; GENERAL\u003cbr\u003e- Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS\u003cbr\u003e- Part 1140; CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS\u003cbr\u003e- Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS\u003cbr\u003e- Part 1143; MINIMUM REQUIRED WARNING STATEMENTS\u003cbr\u003e- Part 1150; USER FEES\u003cbr\u003e- Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT\u003cbr\u003e- Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT\u003cbr\u003e- Part 1240; CONTROL OF COMMUNICABLE DISEASES\u003cbr\u003e- Part 1250; INTERSTATE CONVEYANCE SANITATION\u003cbr\u003e- Parts 1251-1269; Reserved\u003cbr\u003e- Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION\u003cbr\u003e- Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS\u003cbr\u003e- Parts 1272-1299; Reserved\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eAuthor:\u003c\/b\u003e Office of the Federal Register (Cfr)\u003cbr\u003e\u003cb\u003ePublisher:\u003c\/b\u003e Regulations Press\u003cbr\u003e\u003cb\u003ePublished:\u003c\/b\u003e 09\/19\/2017\u003cbr\u003e\u003cb\u003ePages:\u003c\/b\u003e 898\u003cbr\u003e\u003cb\u003eBinding Type:\u003c\/b\u003e Paperback\u003cbr\u003e\u003cb\u003eWeight:\u003c\/b\u003e 2.72lbs\u003cbr\u003e\u003cb\u003eSize:\u003c\/b\u003e 9.21h x 6.14w x 1.77d\u003cbr\u003e\u003cb\u003eISBN:\u003c\/b\u003e 9781298709196\u003c\/p\u003e\u003cp\u003e\u003ci\u003eThis title is not returnable\u003c\/i\u003e\u003cbr\u003e\u003c\/p\u003e","brand":"Regulations Press","offers":[{"title":"Paperback","offer_id":44321882407027,"sku":"9781298709196","price":67.85,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0555\/9255\/0515\/files\/img_34d5937e-86cd-45d1-b668-7e05dad20608.jpg?v=1771505481","url":"https:\/\/bookstorenmore.com\/products\/cfr-21-parts-800-to-1299-food-and-drugs-april-01-2017-volume-8-of-9-9781298709196","provider":"Bookstore N More","version":"1.0","type":"link"}