Medical Device Manufacturer · US , Great Neck , NY

Amplife Corporation - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Recent clearances: AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600, AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100, AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Amplife Corporation General Hospital ✕

2 devices

1-2 of 2

Cleared Nov 19, 2004

AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101

General Hospital · 29d

Cleared Sep 30, 2004

AMPLIFE DIGITAL CLINICAL THERMOMETER

General Hospital · 8d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 25, 2026