ClearanceBrief
510(k) K120672 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

KD-936 FULLY AUTOMATIC WIRELESS BLOOD PRESSURE MONITOR

ApplicantAndon Health Co, Ltd., Princeton NJ, US
DecisionSubstantially Equivalent, Jun 1, 2012
ReceivedMar 5, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120672

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.