ClearanceBrief
510(k) K061935 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

SENSACARE SAW-102 WRIST DIGITAL BLOOD PRESSURE MONITOR

ApplicantSensacare , Ltd., Nei Hu, Taipei, TW
DecisionSubstantially Equivalent, Nov 8, 2006
ReceivedJul 10, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061935

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.