Alertwatch, LLC is one of 18400 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alertwatch, LLC - FDA 510(k) Cleared Devices
Recent clearances: AlertWatch: OR, ALERTWATCH: OR
2
Total
2
Cleared
0
Denied
Alertwatch, LLC has 2 FDA 510(k) cleared medical devices. Based in Clarksville, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Alertwatch, LLC 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, LLC
2 devices