ClearanceBrief
510(k) K894563 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM814F

ApplicantOmron Electronics, Inc., Schaumburg IL, US
DecisionSubstantially Equivalent, Mar 6, 1990
ReceivedJul 21, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894563

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.