Vena Group, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vena Group, LLC has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vena Group, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Vena Group, LLC
1 devices