Critical Alert is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Critical Alert - FDA 510(k) Cleared Devices
Recent clearances: Critical Alert CommonPath Enterprise
1
Total
1
Cleared
0
Denied
Critical Alert has 1 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Critical Alert Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Speed TO Market, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Critical Alert
1 devices