 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
Title 21 - Food and Drugs |
|
|
Chapter I - Food and Drug Administration, Department of Health and Human Services |
|
|
SubChapter H - Medical Devices |
|
|
Part 890 - Physical Medicine Devices |
|
|
Subpart A - General Provisions |
| § 890.1 - Scope. |
| § 890.3 - Effective dates of requirement for premarket approval. |
| § 890.9 - Limitations of exemptions from section 510(k) of the Federal Food, Drug, and Cosmetic Act (the act). |