ClearanceBrief
510(k) K061959 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

MYTECH / HAPPY LIFE / MAXIAIDS ARM BLOOD PRESSURE MONITOR, HPL-301, HPL-302, HPL-310, 180310

ApplicantMytech Technology Co., Ltd., Hsin-Chu City, TW
DecisionSubstantially Equivalent, Aug 22, 2006
ReceivedJul 11, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061959

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.