Amplife Corporation is one of 24307 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amplife Corporation - FDA 510(k) Cleared Devices
Recent clearances: AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600, AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100, AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101
4
Total
4
Cleared
0
Denied
Amplife Corporation has 4 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 4 cleared submissions from 2004 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Amplife Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Amplife Corporation
4 devices
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
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