Medical Device Manufacturer · DE , West Germany

Agfa-Gevaert, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1979

Total

Cleared

Denied

Agfa-Gevaert, Inc. has 3 FDA 510(k) cleared medical devices. Based in West Germany, DE.

Historical record: 3 cleared submissions from 1979 to 1988. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Agfa-Gevaert, Inc. Filter by specialty or product code using the sidebar.

Agfa-Gevaert, Inc. is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Agfa-Gevaert, Inc.

3 devices

1-3 of 3