Alseal is one of 285 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Alseal - FDA 510(k) Cleared Devices
Recent clearances: HQS Introducer (Model 2064-HQS), XCATH, HQS INTRODUCER
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.
Regulatory submissions have been managed by Intertek Testing Services and Smith Associates.
FDA 510(k) Regulatory Record - Alseal
3 devices