ClearanceBrief
510(k) K153707 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Nihon Kohden Vital Sign Telemeter

ApplicantNihon Kohden Corporation, Tokyo, JP
DecisionSubstantially Equivalent, Sep 2, 2016
ReceivedDec 23, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153707

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.