Microlife Corp.
United StatesFDA 510(k) applicant, unverified
Part of Microlife Corporation
- Devices
- 13
What Microlife Corp. makes
Microlife Corp. makes digital infrared ear thermometers, upper arm automatic and manual blood pressure monitors, wrist watch blood pressure monitors, electronic peak flow monitors, and digital basal thermometers.
The devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does Microlife Corp. have in the registry?
The registry currently lists 13 devices for Microlife Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microlife Corp.'s devices?
Among its 13 most recently registered devices, Microlife Corp. has devices listed in FDA 510(k) (13 devices).
What risk classes do Microlife Corp.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Microlife Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microlife Corp. in the registry?
The most recently registered devices listed for Microlife Corp. include MICROLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL IR1DA1, MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL BP3MQ1-2D, MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1 and MICROLIFE UPPER ARM AUTOMATIC BLOOD PRESSURE MONITOR, MODEL BP-3BTO-1, WITH OPTIONAL THERMAL PRINTER, MODEL PR 1KA1.