SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898)
- 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 814—PREMARKET APPROVAL OF MEDICAL DEVICES
- PART 820—QUALITY SYSTEM REGULATION
- PART 821—MEDICAL DEVICE TRACKING REQUIREMENTS
- PART 822—POSTMARKET SURVEILLANCE
- 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