Synapsys SA is one of 295 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Synapsys SA - FDA 510(k) Cleared Devices
Recent clearances: Synapsys Ulmer Video Nystagmograph
1
Total
1
Cleared
0
Denied
Synapsys SA has 1 FDA 510(k) cleared medical devices. Based in Marseille, FR.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Synapsys SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Europe Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Synapsys SA
1 devices