Medical Device Manufacturer · US , Findley , MN

Alertis Medical AS - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

Total

Cleared

Denied

Alertis Medical AS has 1 FDA 510(k) cleared medical devices. Based in Findley, US.

Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Alertis Medical AS Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Alertis Medical AS

1 devices

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