Gynecare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GYNECARE VERSAPOINT G-VAP ELECTRODE, VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA), SCUBA SYSTEM
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Gynecare, Inc. Obstetrics & Gynecology ✕
3 devices