Alertwatch, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alertwatch, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AlertWatch:AC, AlertWatch:OB
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: Obstetrics & Gynecology.
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.
FDA 510(k) Regulatory Record - Alertwatch, Inc.
2 devices