ClearanceBrief
510(k) K120673 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

DIGITAL AUTOMATIC WRIST BLOOD PRESSURE MONITOR WBPM15 SERIES

ApplicantGrandway Technology (Shenzhen) Limited, Shenzhen, CN
DecisionSubstantially Equivalent, Feb 14, 2013
ReceivedMar 5, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120673

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.