Surgitek - FDA 510(k) Cleared Devices
Recent clearances: QUADRA-COIL URETERAL STENT, OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM, RIGHT ANGLE UROLOGIC LASER FIBER
29
Total
28
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgitek General Hospital ✕
1 devices