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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter H - Medical Devices |
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Part 860 - Medical Device Classification Procedures |
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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 - xxx |
| § 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. |