Medical Device Manufacturer · US , Madison , WI

Phasein AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

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

Historical record: 5 cleared submissions from 2007 to 2012. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Phasein AB

5 devices

1-5 of 5