Trans Vascular Incorporated is one of 25736 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trans Vascular Incorporated - FDA 510(k) Cleared Devices
Recent clearances: CROSSPOINT TRANSACCESS CATHETER, MODEL TA-XP-001, CROSSPOINT TRANSACCESS CATHETER
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Trans Vascular Incorporated
2 devices