Reports from the Center for Devices and Radiological Health and individual CDRH offices.
Please note: Some web links (URLs) embedded within these reports are no longer valid. If you find a link that does not work, please try searching for the information using document titles or key words.
- FDA Has Taken Steps to Strengthen the 510(k) Program - November 26, 2018
- CDRH Medical Device Enforcement and Quality Report - November 21, 2018