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