Medical Device Manufacturer · US , Menlo Park , CA

Guidant Cardiac and Vascular Surgery - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1997

Recent clearances: ANCURE SHEATH MODEL # 40315, 40320, 40325, GUIDANT RETRIEVER DEVICE, ANCURE LLIAC BALLOON CATHETER

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Guidant Cardiac and Vascular Surgery Radiology ✕

1 devices

1-1 of 1

Cleared Apr 21, 1997

EVT MARKER BOARD

Radiology · 62d