Medical Device Manufacturer · US , Douglasville , GA

Heart Alert, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Recent clearances: P.H.D. - PERSONAL HEART DEVICE MODEL 5258

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Heart Alert, Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared May 15, 1997

P.H.D. - PERSONAL HEART DEVICE MODEL 5258

Cardiovascular · 227d