Medical Device Manufacturer · SE , V?ster?s

Toul Meditech AB - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2016

Total

Cleared

Denied

Toul Meditech AB has 3 FDA 510(k) cleared medical devices. Based in V?ster?s, SE.

Historical record: 3 cleared submissions from 2016 to 2019. Primary specialty: General Hospital.

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

FDA 510(k) cleared devices by Toul Meditech AB

3 devices

1-3 of 3