Heart Alert, Inc. is one of 13224 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Heart Alert, Inc. - FDA 510(k) Cleared Devices
Recent clearances: P.H.D. - PERSONAL HEART DEVICE MODEL 5258
1
Total
1
Cleared
0
Denied
Heart Alert, Inc. has 1 FDA 510(k) cleared medical devices. Based in Douglasville, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Heart Alert, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Heart Alert, Inc.
1 devices