Medical Device Manufacturer · US , Bellevue , WA

Coopervision-Cilco - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Coopervision-Cilco has 2 FDA 510(k) cleared medical devices. Based in Bellevue, US.

Historical record: 2 cleared submissions from 1988 to 1988. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Coopervision-Cilco Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Coopervision-Cilco

2 devices

1-2 of 2