Medical Device Manufacturer · US , Greenville , SC

Signalife, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

Recent clearances: FIDELITY 200 CARDIAC EVENT RECORDER

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Nov 21, 2007

FIDELITY 200 CARDIAC EVENT RECORDER

Cardiovascular · 202d