Code of Federal Regulations (Last Updated: May 6, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter A - General |
Part 5 - Organization |
Subpart I - Product Designation; Redelegations of Authority |
§ 5.700 - Authority relating to determination of product primary jurisdiction. |
§ 5.701 - Premarket approval of a product that is or contains a biologic, a device, or a drug. |