21 CFR Part 803 - MEDICAL DEVICE REPORTING
- Subpart A - General Provisions (§§ 803.1 - 803.19)
- Subpart B - Generally Applicable Requirements for Individual Adverse Event Reports (§§ 803.20 - 803.23)
- Subpart C - User Facility Reporting Requirements (§§ 803.30 - 803.33)
- Subpart D - Importer Reporting Requirements (§§ 803.40 - 803.42)
- Subpart E - Manufacturer Reporting Requirements (§§ 803.50 - 803.58)
{'United States Code': [{'Title': '21', 'Section': '352', 'headtext': ' Misbranded drugs and devices', 'cleanpath': '/uscode/text/21/352'}, {'Title': '21', 'Section': '360', 'headtext': ' Registration of producers of drugs or devices', 'cleanpath': '/uscode/text/21/360'}, {'Title': '21', 'Section': '360i', 'headtext': ' Records and reports on devices', 'cleanpath': '/uscode/text/21/360i'}, {'Title': '21', 'Section': '360j', 'headtext': ' General provisions respecting control of devices intended for human use', 'cleanpath': '/uscode/text/21/360j'}, {'Title': '21', 'Section': '371', 'headtext': ' Regulations and hearings', 'cleanpath': '/uscode/text/21/371'}, {'Title': '21', 'Section': '374', 'headtext': ' Inspection', 'cleanpath': '/uscode/text/21/374'}], 'Statutes at Large': [], 'Public Laws': [], 'Presidential Documents': []}