Bayer Corp., Agfa Div. is one of 20418 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bayer Corp., Agfa Div. - FDA 510(k) Cleared Devices
Recent clearances: CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMPACT PLUS, CURIX COMS, ADC COMPACT (AGFA DIAGNOSTIC CENTER), LR 5200 LASER FILM RECORDER
3
Total
3
Cleared
0
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