Vasc-Alert, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vasc-Alert, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vasc-Alert, LLC has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vasc-Alert, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vasc-Alert, LLC
1 devices