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 809 - In Vitro Diagnostic Products for Human Use |
Subpart A - General Provisions |
§ 809.3 - Definitions. |
§ 809.4 - Confidentiality of submitted information. |
§ 809.5 - Exemption from batch certification requirements for in vitro antibiotic susceptibility devices subject to section 507 of the act. |
§ 809.6 - Conditions on the effectiveness of exemptions of antibiotic susceptibility devices from batch certification requirements. |