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 Cardiovascular ✕

2 devices

1-2 of 2

Cleared Mar 04, 2005

AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600

Cardiovascular · 14d

Cleared Jan 27, 2005

AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100

Cardiovascular · 35d

Data Source

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

Last updated: Sep 25, 2026