Medical Device Manufacturer · US , Bothell , WA

Aqueduct Critical Care, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2016

Total

Cleared

Denied

Aqueduct Critical Care, Inc. has 4 FDA 510(k) cleared medical devices. Based in Bothell, US.

Historical record: 4 cleared submissions from 2016 to 2018. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Aqueduct Critical Care, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Aqueduct Critical Care, Inc.

4 devices

1-4 of 4