Microlife Corp. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Microlife Corp. has 13 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 13 cleared submissions from 2000 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Microlife Corp. Filter by specialty or product code using the sidebar.
13 devices
Cleared
May 13, 2013
MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+...
Cardiovascular
307d
Cleared
May 13, 2008
MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2D
Cardiovascular
95d
Cleared
Dec 20, 2007
MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)
Cardiovascular
17d
Cleared
Dec 20, 2007
MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3MK1-3 (BP W100)
Cardiovascular
17d
Cleared
Jul 21, 2004
MICROLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL BP-3BTO-AP
Cardiovascular
55d
Cleared
Nov 14, 2003
MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100
Anesthesiology
228d
Cleared
Sep 12, 2003
MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921
Obstetrics & Gynecology
169d
Cleared
Jun 28, 2002
MICROLIFE WRIST WATCH BLOOD PRESSURE, MODEL BP-3BU1-5, WITH OPTIONAL THERMAL...
Cardiovascular
65d
Cleared
Mar 12, 2002
MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
General Hospital
6d
Cleared
Jan 17, 2002
MICROLIFE UPPER ARM AUTOMATIC BLOOD PRESSURE MONITOR, MODEL BP-3BTO-1, WITH...
Cardiovascular
90d
Cleared
Nov 14, 2000
MICROLIFE DIGITAL INFRARED EAR THERMOMETER, IR1DAI, IR1DB1, IR1DD1
General Hospital
22d
Cleared
Aug 22, 2000
MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DA1
General Hospital
148d