21 CFR Part 872 - DENTAL DEVICES
- Subpart A - General Provisions (§§ 872.1 - 872.9)
- Subpart B - Diagnostic Devices (§§ 872.1500 - 872.2060)
- Subpart C [Reserved]
- Subpart D - Prosthetic Devices (§§ 872.3060 - 872.3980)
- Subpart E - Surgical Devices (§§ 872.4120 - 872.4920)
- Subpart F - Therapeutic Devices (§§ 872.5410 - 872.5580)
- Subpart G - Miscellaneous Devices (§§ 872.6010 - 872.6890)
Source:
52 FR 30097, Aug. 12, 1987, unless otherwise noted.
Editorial Note:
Nomenclature changes to part 872 appear at 73 FR 35341, June 23, 2008.
{'United States Code': [{'Title': '21', 'Section': '351', 'headtext': ' Adulterated drugs and devices', 'cleanpath': '/uscode/text/21/351'}, {'Title': '21', 'Section': '360', 'headtext': ' Registration of producers of drugs or devices', 'cleanpath': '/uscode/text/21/360'}, {'Title': '21', 'Section': '360c', 'headtext': ' Classification of devices intended for human use', 'cleanpath': '/uscode/text/21/360c'}, {'Title': '21', 'Section': '360e', 'headtext': ' Premarket approval', 'cleanpath': '/uscode/text/21/360e'}, {'Title': '21', 'Section': '360j', 'headtext': ' General provisions respecting control of devices intended for human use', 'cleanpath': '/uscode/text/21/360j'}, {'Title': '21', 'Section': '360l', 'headtext': ' Postmarket surveillance', 'cleanpath': '/uscode/text/21/360l'}, {'Title': '21', 'Section': '371', 'headtext': ' Regulations and hearings', 'cleanpath': '/uscode/text/21/371'}], 'Statutes at Large': [], 'Public Laws': [], 'Presidential Documents': []}