Medical Device Manufacturer · CH , Zurich

Oculocare Medical AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

Oculocare Medical AG has 1 FDA 510(k) cleared medical devices. Based in Zurich, CH.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Oculocare Medical AG Filter by specialty or product code using the sidebar.

1 devices
1–1 of 1
Filters
Filter by Specialty
All1 Ophthalmic 1