Eurobio is one of 160 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Eurobio - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Eurobio has 1 FDA 510(k) cleared medical devices. Based in Les Ulis, FR.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eurobio Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eurobio
1 devices