Medical Device Manufacturer · US , Chicago , IL

Innovision A/S - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2006

Total

Cleared

Denied

Innovision A/S has 4 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 4 cleared submissions from 2006 to 2011. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Innovision A/S Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Innovision A/S

4 devices

1-4 of 4