Alertwatch, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Biologics Consulting Group, Inc. as regulatory consultant.
2 devices