ClearanceBrief
510(k) K011352 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

ROSSMAX SMARTINFLATE CARDIOPRO, MODEL 1000I AND MODEL 3000I BLOOD PRESSURE MONITORS

ApplicantRossmax International , Ltd., Taipei, TW
DecisionSubstantially Equivalent, Jul 20, 2001
ReceivedMay 3, 2001
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K011352

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.