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Euro-Am Pharma, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K912620OPOMAT MANUAL RESUSCITATOR VENTILATORDecember 4, 1991
K900588ACU-BAND ACCUPRESSURE WRIST BANDFebruary 22, 1990