Medical Device Manufacturer · CA , Quebec

Opsens - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Opsens has 1 FDA 510(k) cleared medical devices. Based in Quebec, CA.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.

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

Opsens is one of 185 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Opsens

1 devices

1-1 of 1