Microlife Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K122013MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+ (BP4GAPO-2M)May 13, 2013
K080337MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2DMay 13, 2008
K073397MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)December 20, 2007
K073398MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3MK1-3 (BP W100)December 20, 2007
K041411MICROLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL BP-3BTO-APJuly 21, 2004
K031024MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100November 14, 2003
K030961MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921September 12, 2003
K021305MICROLIFE WRIST WATCH BLOOD PRESSURE, MODEL BP-3BU1-5, WITH OPTIONAL THERMAL PRINTERJune 28, 2002
K020725MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1March 12, 2002
K013485MICROLIFE UPPER ARM AUTOMATIC BLOOD PRESSURE MONITOR, MODEL BP-3BTO-1, WITH OPTIONAL THERMAL PRINTERJanuary 17, 2002
K003308MICROLIFE DIGITAL INFRARED EAR THERMOMETER, IR1DAI, IR1DB1, IR1DD1November 14, 2000
K000969MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DA1August 22, 2000
K001182MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1August 1, 2000