CFR 21, Parts 800 to 1299, Food and Drugs, April 01, 2017 (Volume 8 of 9)

Code of Federal Regulations Title 21, Volume 8, April 1, 2017 contains regulations governing Food and Drugs and may also be referenced as:- Code of Federal Regulations Title 21, Volume 8, April 1, 2017- CFR Title 21- CFR 21, Food and Drugs- CFR 21, Parts 800 to 1299, Food and DrugsThis volume contains Parts 800 to 1299:- Part 800; GENERAL- Part 801; LABELING- Part 803; MEDICAL DEVICE REPORTING- 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 1100; TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY- Part 1105; GENERAL- Part 1105; GENERAL- Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS- Part 1140; CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS- Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS- Part 1143; MINIMUM REQUIRED WARNING STATEMENTS- 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