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. |
|
|