Intervascular Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Intervascular Sas - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Intervascular Sas has 1 FDA 510(k) cleared medical devices. Based in La Ciotat, FR.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intervascular Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intervascular Sas
1 devices