21 CFR Part 860in-force
21 CFR Part 860 — Medical Device Classification Procedures (FDA — Food and Drugs)
21 CFR part 860
Summary
US eCFR 21 CFR Part 860 (Medical Device Classification Procedures) — FDA — Food and Drugs.
Scope
US Code of Federal Regulations part — reference resource for fda — food and drugs.
Expert analysis
SaveOur compliance experts are preparing a detailed analysis for this regulation. Check back soon.
Want this analysis for your product?
Enter your product features once — ComplyMatrix maps all applicable EU regulations, obligations and testing requirements in minutes.