Medical Device Manufacturer · US , Washington , DC

Jolife AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Jolife AB has 5 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 5 cleared submissions from 2006 to 2018. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Jolife AB

5 devices

1-5 of 5