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Gynopharma, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K903001SLIMCATH (TM)June 25, 1991
K903002PROBET (TM)April 5, 1991