ClearanceBrief
510(k) K882393 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

DIGITAL BLOOD PRESSURE MONITOR MODEL HEM-703CP

ApplicantOmron Electronics, Inc., Schaumburg IL, US
DecisionSubstantially Equivalent, Aug 30, 1988
ReceivedJun 10, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882393

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.