ClearanceBrief
510(k) K981702 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

AUTOMATIC DIGITAL ELECTRONIC WRIST BLOOD PRESSURE MONITOR MODEL NUMBER WS-300

ApplicantNihon Seimitsu Sokki Co., Ltd., Smithfield VA, US
DecisionSubstantially Equivalent, Mar 5, 1999
ReceivedMay 14, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981702

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.