Federal (United States) · Regulations
Subpart C
8 sections
8 sections
- 21 C.F.R. § 860.120General.
- 21 C.F.R. § 860.123Reclassification petition: Content and form.
- 21 C.F.R. § 860.125Consultation with panels.
- 21 C.F.R. § 860.130General procedures under section 513(e) of the Federal Food, Drug, and Cosmetic Act.
- 21 C.F.R. § 860.132Procedures when the Commissioner initiates a performance standard or premarket approval proceeding under section 514(b) or 515(b) of the Federal Food, Drug, and Cosmetic Act.
- 21 C.F.R. § 860.133Procedures when the Commissioner initiates a proceeding to require premarket approval under section 515(b) of the Federal Food, Drug, and Cosmetic Act.
- 21 C.F.R. § 860.134Procedures for reclassification of “postamendments devices” under section 513(f)(3) of the Federal Food, Drug, and Cosmetic Act.
- 21 C.F.R. § 860.136Procedures for transitional products under section 520(l) of the Federal Food, Drug, and Cosmetic Act.