510(k) K222979

Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5W by Microlife Intellectual Property GmbH — Product Code DXN

K222979 is an FDA 510(k) premarket notification submitted by Microlife Intellectual Property GmbH for the device "Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5W". The FDA issued a decision of Substantially Equivalent on May 19, 2023. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Microlife Intellectual Property GmbH has at least 10 other 510(k) clearances on record.