Medical Device Manufacturer · US , Menlo Park , CA

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

7 submissions · 7 cleared · Since 1997

Total

Cleared

Denied

Guidant Cardiac and Vascular Surgery has 7 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 7 cleared submissions from 1997 to 2002. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Guidant Cardiac and Vascular Surgery Filter by specialty or product code using the sidebar.

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

7 devices

1-7 of 7