Publisher's Synopsis
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
