FDA 510(k) Applications Submitted by BAYER CORP., AGFA DIV.

FDA 510(k) Number Submission Date Device Name Applicant
K981280 04/08/1998 CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMPACT PLUS, CURIX COMS BAYER CORP., AGFA DIV.
K964414 11/05/1996 LR 5200 LASER FILM RECORDER BAYER CORP., AGFA DIV.
K974597 12/09/1997 ADC COMPACT (AGFA DIAGNOSTIC CENTER) BAYER CORP., AGFA DIV.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact