Alseal is one of 151 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Alseal - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Alseal has 3 FDA 510(k) cleared medical devices. Based in Besancon, FR.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Alseal Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alseal
3 devices