PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES
- SUBPART A—General (§814.1 to §814.19)
- SUBPART B—Premarket Approval Application (PMA) (§814.20 to §814.39)
- SUBPART C—FDA Action on a PMA (§814.40 to §814.47)
- SUBPART E—Postapproval Requirements (§814.80 to §814.84)
- SUBPART H—Humanitarian Use Devices (§814.100 to §814.126)