ClearanceBrief
510(k) K252685 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-61D2L, DBP-61D2L-P, DBP-63D2L, DBP-63D2L-P, DBP-61D9L,DBP-61D9L-P, DBP-63D9L, DBP-63D9L-P, DBP-62F4L, DBP-62F4B, DBP-61F4,DBP-61F4L, DBP-61F4-P, DBP-61F4L-P, DBP-62F4L-P, DBP-62F4B-P)

ApplicantJoytech Healthcare Co. , Ltd., Hangzhou, CN
DecisionSubstantially Equivalent, Feb 13, 2026
ReceivedAug 26, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252685

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.