Guidant Corporation - FDA 510(k) Cleared Devices
Recent clearances: HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE, OMNILINK .035 BILIARY STENT SYSTEM, RX HERCULINK ELITE BILIARY STENT SYSTEM
15
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Guidant Corporation General & Plastic Surgery ✕
2 devices