Oculomotor Technologies - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Oculomotor Technologies has 1 FDA 510(k) cleared medical devices. Based in Princeton, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculomotor Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Oculomotor Technologies
1 devices