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Bayer Corp., Agfa Div.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K981280
CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMP
April 30, 1998
K974597
ADC COMPACT (AGFA DIAGNOSTIC CENTER)
March 9, 1998
K964414
LR 5200 LASER FILM RECORDER
January 27, 1997