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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 A - General |
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Part 3 - Product Jurisdiction |
| Subpart A - Assignment of Agency Component for Review of Premarket Applications |
| § 3.1 - Purpose. |
| § 3.2 - Definitions. |
| § 3.3 - Scope. |
| § 3.4 - Designated agency component. |
| § 3.5 - Procedures for identifying the designated agency component. |
| § 3.6 - Product jurisdiction officer. |
| § 3.7 - Request for designation. |
| § 3.8 - Letter of designation. |
| § 3.9 - Effect of letter of designation. |
| § 3.10 - Stay of review time. |
| Subpart B - XXX |