Medical Device Manufacturer · US , Ann Arbor , MI

Alertwatch, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Alertwatch, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.

Last cleared in 2021. Active since 2018. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Alertwatch, Inc.

2 devices

1-2 of 2