Microlife Corp.
Microlife Corp. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2013.
Top product codes for Microlife Corp.
Recent clearances by Microlife Corp.
- K122013 — MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+ (BP4GAPO-2M)
- K080337 — MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2D
- K073397 — MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)
- K073398 — MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3MK1-3 (BP W100)
- K041411 — MICROLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL BP-3BTO-AP
- K031024 — MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100
- K030961 — MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921
- K021305 — MICROLIFE WRIST WATCH BLOOD PRESSURE, MODEL BP-3BU1-5, WITH OPTIONAL THERMAL PRINTER
- K020725 — MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DE1
- K013485 — MICROLIFE UPPER ARM AUTOMATIC BLOOD PRESSURE MONITOR, MODEL BP-3BTO-1, WITH OPTIONAL THERMAL PRINTER, MODEL PR 1KA1
- K003308 — MICROLIFE DIGITAL INFRARED EAR THERMOMETER, IR1DAI, IR1DB1, IR1DD1
- K000969 — MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DA1
- K001182 — MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1
Data sourced from openFDA. This site is unofficial and independent of the FDA.