Vitreq BV - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Vitreq BV has 2 FDA 510(k) cleared medical devices. Based in Vierpolders, NL.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vitreq BV Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Vitreq BV
2 devices