Medical Device Manufacturer · US , Moorepark , CA

Koros USA, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2007

Total

Cleared

Denied

Koros USA, Inc. has 4 FDA 510(k) cleared medical devices. Based in Moorepark, US.

Historical record: 4 cleared submissions from 2007 to 2013. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Koros USA, Inc. Filter by specialty or product code using the sidebar.

4 devices

1–4 of 4