FDA 2121 CFR Part 860
Medical Device Classification Procedures
United StatesFDAClassification
What this code is
21 CFR Part 860 is the official FDA identifier for “Medical Device Classification Procedures”. 21 CFR Part 860 is the official identifier FDA uses for this instrument.
- Instrument
- 21
- Full name
- 21 CFR Part 860
- Category
- Classification
Source links
- Authority source
- English
- Readable HTML
- 23 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 Classification Procedures
Current eCFR Part 860 classification procedures, including De Novo.
21 CFR Part 860 is the official identifier FDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.