Medical Device Manufacturer · SE , Linkoping

Context Vision AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Total

Cleared

Denied

Context Vision AB has 2 FDA 510(k) cleared medical devices. Based in Linkoping, SE.

Historical record: 2 cleared submissions from 2000 to 2003. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Context Vision AB

2 devices

1-2 of 2