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 O.
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Parts 800 to 1299 |