21 CFR Part 814 - PREMARKET APPROVAL OF MEDICAL DEVICES
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- Subpart A—General (§§ 814.1 - 814.19)
- Subpart B—Premarket Approval Application (PMA) (§§ 814.20 - 814.39)
- Subpart C—FDA Action on a PMA (§§ 814.40 - 814.47)
- Subpart D—Administrative Review [Reserved]
- Subpart E—Postapproval Requirements (§§ 814.80 - 814.84)
- Subparts F-G [Reserved]
- Subpart H—Humanitarian Use Devices (§§ 814.100 - 814.126)