Laboratoire Villanova is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Laboratoire Villanova - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Laboratoire Villanova has 1 FDA 510(k) cleared medical devices. Based in Le Touquet, FR.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Laboratoire Villanova Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laboratoire Villanova
1 devices