ClearanceBrief
510(k) K122259 ยท DXQ Blood Pressure Cuff

BLOOD PRESSURE MONITOR WITH STETHOSCOPE

ApplicantHangzhou Reli-On Co., Ltd., Echo OR, US
DecisionSubstantially Equivalent, Sep 24, 2012
ReceivedJul 27, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122259

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.