ClearanceBrief
510(k) K912588 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

AUTOMATIC DIGITAL BLOOD PRESSURE METERS, MODELS

ApplicantSein Electronics Co., Ltd., Mahwah NJ, US
DecisionSubstantially Equivalent, Dec 19, 1991
ReceivedJun 12, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912588

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.