FDA 2121 CFR Part 812
Investigational Device Exemptions
United StatesFDAClinical Trials
What this code is
21 CFR Part 812 is the official FDA identifier for “Investigational Device Exemptions”. 21 CFR Part 812 is the official identifier FDA uses for this instrument.
- Instrument
- 21
- Full name
- 21 CFR Part 812
- Category
- Clinical Trials
Source links
- Authority source
- English
- Readable HTML
- 33 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
Investigational Device Exemptions
Current eCFR Part 812 investigational device exemption requirements.
21 CFR Part 812 is the official identifier FDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.