Medical Device Manufacturer · SE , Jarfalla

Perimed AB - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

Total

Cleared

Denied

Perimed AB has 4 FDA 510(k) cleared medical devices. Based in Jarfalla, SE.

Historical record: 4 cleared submissions from 2001 to 2016. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Perimed AB

4 devices

1-4 of 4