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 Drugs This 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