510(k) K242721

Upper Arm Electronic Blood Pressure Monitor (FC-BP103, FC-BP106, FC-BP113, FC-BP120, FC-BP121, FC-BP130, FC-BP131) by Shenzhen Finicare Co., Ltd. — Product Code DXN

K242721 is an FDA 510(k) premarket notification submitted by Shenzhen Finicare Co., Ltd. for the device "Upper Arm Electronic Blood Pressure Monitor (FC-BP103, FC-BP106, FC-BP113, FC-BP120, FC-BP121, FC-BP130, FC-BP131)". The FDA issued a decision of Substantially Equivalent on October 4, 2024. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Shenzhen Finicare Co., Ltd. has at least 5 other 510(k) clearances on record.