ClearanceBrief
510(k) K133125 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

WITHINGS BLOOD PRESURE MONITOR

ApplicantWithings, Issy Les Moulineaux, FR
DecisionSubstantially Equivalent, Mar 24, 2014
ReceivedSep 30, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133125

DateFirm and productCodeLinked 510(k)
Jun 11, 2018Withings Sas
Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Completed
DXNNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.