Guidant Corp. - FDA 510(k) Cleared Devices
71
Total
56
Cleared
0
Denied
FDA 510(k) Regulatory Record - Guidant Corp. General & Plastic Surgery ✕
4 devices
Cleared
Jul 27, 2006
FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05
General & Plastic Surgery
24d
Cleared
May 14, 2003
GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM
General & Plastic Surgery
84d
Cleared
Nov 12, 2002
ESSEX ENDOSCOPE, MODEL SXD-1000
General & Plastic Surgery
15d
Cleared
Jan 10, 2002
7MM EXTENDED LENGTH ENDOSCOPE,DISSECTION TIPS, MODELS VH-1111, VH-1114
General & Plastic Surgery
15d