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-NumberDeviceDate
K981280CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMPApril 30, 1998
K974597ADC COMPACT (AGFA DIAGNOSTIC CENTER)March 9, 1998
K964414LR 5200 LASER FILM RECORDERJanuary 27, 1997