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Bayer Corp., Agfa Div.

FDA Regulatory Profile

Bayer Corp., Agfa Div. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 30, 1998.

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

FDA data resources