1 research outputs found
United States food and drug administration
- Author
- 515 Program Initiative (Reclassification of Preamendments Class III 510(k)s) Project Status
- Center for Devices and Radiological Health
- De Novo Classification Request
- Device Advice: Comprehensive Regulatory Assistance
- Investigational Device Exemption (IDE)
- Laws Enforced by FDA
- Medical Device Databases
- Medical Device Exemptions 510(k) and GMP Requirements
- Medical Device User Fee Amendments (MDUFA)
- Reorganization of The Center for Devices and Radiological Health
- Search Product Classification
- Standards and Conformity Assessment Program
- US Food and Drug Administration (FDA)
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2020
- Field of study
No full text
