Gynescope Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K902658GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODESSeptember 19, 1990
K902657GYNESCOPE LAPAROSCOPIC FORCEPSSeptember 19, 1990
K901530WALLACE INTRAUTERINE INSEMINATION CATHETERJuly 23, 1990
K902655GYNESCOPE LAPAROSCOPESJuly 13, 1990
K902656GYNESCOPE LAPAROSCOPIC TROCARS AND SLEEVESJune 29, 1990
K902019MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPSJune 7, 1990
K902049CROAK OVARIAN BIOPSY FORCEPJune 7, 1990
K900878OTT INSUFFLATION FILTER TUBINGMay 7, 1990
K895225GYNECOLOGICAL INSTRUMENTATIONMarch 5, 1990