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.

Bayer Corp., Agfa Div. is one of 6936 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

3 devices

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