SUBCHAPTER H — MEDICAL DEVICES  


Part 870 - CARDIOVASCULAR DEVICES
Part 814 - PREMARKET APPROVAL OF MEDICAL DEVICES
Part 800 - GENERAL
Part 880 - GENERAL HOSPITAL AND PERSONAL USE DEVICES
Part 807 - ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Part 890 - PHYSICAL MEDICINE DEVICES
Part 830 - UNIQUE DEVICE IDENTIFICATION
Part 864 - HEMATOLOGY AND PATHOLOGY DEVICES
Part 898 - PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
Part 809 - IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Part 808 - EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
Part 820 - QUALITY SYSTEM REGULATION
Part 874 - EAR, NOSE, AND THROAT DEVICES
Part 806 - MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Part 812 - INVESTIGATIONAL DEVICE EXEMPTIONS
Part 878 - GENERAL AND PLASTIC SURGERY DEVICES
Part 866 - IMMUNOLOGY AND MICROBIOLOGY DEVICES
Part 882 - NEUROLOGICAL DEVICES
Part 822 - POSTMARKET SURVEILLANCE
Part 886 - OPHTHALMIC DEVICES
Part 810 - MEDICAL DEVICE RECALL AUTHORITY
Part 813 - [Reserved]
Part 868 - ANESTHESIOLOGY DEVICES
Part 860 - MEDICAL DEVICE CLASSIFICATION PROCEDURES
Part 888 - ORTHOPEDIC DEVICES
Part 895 - BANNED DEVICES
Part 821 - MEDICAL DEVICE TRACKING REQUIREMENTS
Part 803 - MEDICAL DEVICE REPORTING
Part 892 - RADIOLOGY DEVICES
Part 861 - PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
Part 884 - OBSTETRICAL AND GYNECOLOGICAL DEVICES
Part 801 - LABELING
Part 872 - DENTAL DEVICES
Part 862 - CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
Part 876 - GASTROENTEROLOGY-UROLOGY DEVICES