ClearanceBrief
510(k) K993542 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL V46

ApplicantRossmax International , Ltd., Taipei, TW
DecisionSubstantially Equivalent, Dec 29, 1999
ReceivedOct 19, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K993542

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.