Gynemetrics, Inc.

FDA Regulatory Profile

Gynemetrics, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 16, 1981.

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
K802315UTERINE SOUNDJanuary 12, 1981
K802313UTERINE CURETTEJanuary 12, 1981