Medical Device Manufacturer · US , Sunnyvale , CA

Avantec Vascular Corp. - FDA 510(k) Cleared Devices

3 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Avantec Vascular Corp. has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 1 cleared submissions from 2003 to 2004. Primary specialty: Gastroenterology & Urology.

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

Avantec Vascular Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Avantec Vascular Corp.

3 devices

1-3 of 3