Subchap H — Medical Devices
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- Pt. 800 General §§800.10 to 800.75
- Pt. 801 Labeling §§801.1 to 801.437
- Pt. 803 Medical Device Reporting §§803.1 to 803.58
- Pt. 806 Medical Devices; Reports of Corrections and Removals §§806.1 to 806.40
- Pt. 807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices §§807.3 to 807.100
- Pt. 808 Exemptions from Federal Preemption of State and Local Medical Device Requirements §§808.1 to 808.57-808.101
- Pt. 809 In Vitro Diagnostic Products for Human Use §§809.3 to 809.40
- Pt. 810 Medical Device Recall Authority §§810.1 to 810.18
- Pt. 812 Investigational Device Exemptions §§812.1 to 812.150
- Pt. 813 Part 813 [reserved]
- Pt. 814 Premarket Approval of Medical Devices §§814.1 to 814.126
- Pt. 820 Quality Management System Regulation §§820.1 to 820.45
- Pt. 821 Medical Device Tracking Requirements §§821.1 to 821.60
- Pt. 822 Postmarket Surveillance §§822.1 to 822.38
- Pt. 830 Unique Device Identification §§830.3 to 830.360
- Pt. 860 Medical Device Classification Procedures §§860.1 to 860.260
- Pt. 861 Procedures for Performance Standards Development §§861.1 to 861.38
- Pt. 862 Clinical Chemistry and Clinical Toxicology Devices §§862.1 to 862.3970
- Pt. 864 Hematology and Pathology Devices §§864.1 to 864.9900
- Pt. 866 Immunology and Microbiology Devices §§866.1 to 866.6110
- Pt. 868 Anesthesiology Devices §§868.1 to 868.6885
- Pt. 870 Cardiovascular Devices §§870.1 to 870.5925
- Pt. 872 Dental Devices §§872.1 to 872.6890
- Pt. 874 Ear, Nose, and Throat Devices §§874.1 to 874.6000
- Pt. 876 Gastroenterology-Urology Devices §§876.1 to 876.5990
- Pt. 878 General and Plastic Surgery Devices §§878.1 to 878.5910
- Pt. 880 General Hospital and Personal Use Devices §§880.1 to 880.6992
- Pt. 882 Neurological Devices §§882.1 to 882.5970
- Pt. 884 Obstetrical and Gynecological Devices §§884.1 to 884.6200
- Pt. 886 Ophthalmic Devices §§886.1 to 886.5933
- Pt. 888 Orthopedic Devices §§888.1 to 888.5980
- Pt. 890 Physical Medicine Devices §§890.1 to 890.5975
- Pt. 892 Radiology Devices §§892.1 to 892.6510
- Pt. 895 Banned Devices §§895.1 to 895.105
- Pt. 898 Performance Standard for Electrode Lead Wires and Patient Cables §§898.11 to 898.14