ClearanceBrief
510(k) K242193 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

Arm Type Blood Pressure Monitor (BPM82)

ApplicantAvita Corporation, New Taipei City, TW
DecisionSubstantially Equivalent, Oct 22, 2024
ReceivedJul 26, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242193

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.