Eureduc is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Eureduc - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Eureduc has 2 FDA 510(k) cleared medical devices. Based in Antony, FR.
Historical record: 2 cleared submissions from 1996 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Eureduc Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eureduc
2 devices