FDA 2121 CFR Part 803
Medical Device Reporting
United StatesFDAVigilance
What this code is
21 CFR Part 803 is the official FDA identifier for “Medical Device Reporting”. 21 CFR Part 803 is the official identifier FDA uses for this instrument.
- Instrument
- 21
- Full name
- 21 CFR Part 803
- Category
- Vigilance
Source links
- Authority source
- English
- Readable HTML
- 26 articles · 1 language version
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
- Published
- —
- Effective
- —
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About this regulation
Medical Device Reporting
Current eCFR Part 803 medical device reporting requirements.
21 CFR Part 803 is the official identifier FDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.