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Gynemetrics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K811568CERVICAL DILATORJuly 16, 1981
K803210MENSTRUAL ASPIRATION KITSJanuary 28, 1981
K802313UTERINE CURETTEJanuary 12, 1981
K802315UTERINE SOUNDJanuary 12, 1981