Microlife Corp. - FDA 510(k) Cleared Devices
Recent clearances: MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+ (BP4GAPO-2M), MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2D, MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)
13
Total
13
Cleared
0
Denied
FDA 510(k) Regulatory Record - Microlife Corp. General Hospital ✕
3 devices
Cleared
Mar 12, 2002
MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
General Hospital
6d
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