Medical Device Manufacturer · US , Ridgefield Park , NJ

Bayer Corp., Agfa Div. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

Total

Cleared

Denied

Bayer Corp., Agfa Div. has 3 FDA 510(k) cleared medical devices. Based in Ridgefield Park, US.

Historical record: 3 cleared submissions from 1997 to 1998. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Bayer Corp., Agfa Div. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bayer Corp., Agfa Div.

3 devices

1-3 of 3