Medical Device Manufacturer · US , Menlo Park , CA

Trans Vascular Incorporated - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Trans Vascular Incorporated has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Trans Vascular Incorporated Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Trans Vascular Incorporated

2 devices

1-2 of 2