ClearanceBrief
510(k) K131346 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR

ApplicantMicrolife Intellectual Property GmbH, Great Neck NY, US
DecisionSubstantially Equivalent, Jun 6, 2013
ReceivedMay 9, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K131346

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.