Medical Device Manufacturer · US , St. Paul , MN

Guidant Corporation - FDA 510(k) Cleared Devices

15 submissions · 12 cleared · Since 2003

15

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - Guidant Corporation General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Sep 21, 2005

GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000

General & Plastic Surgery · 30d

Cleared Aug 20, 2004

GUIDANT VASOVIEW 6 HARVESTING CANNULA, MODEL VH-2000

General & Plastic Surgery · 28d