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Bayer Corp., Agfa Div.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K981280 CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMPACT PLUS, CURIX COMSIXW1998-04-30 View
510(k) K974597 ADC COMPACT (AGFA DIAGNOSTIC CENTER)KPR1998-03-09 View
510(k) K964414 LR 5200 LASER FILM RECORDERLMC1997-01-27 View
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