ClearanceBrief
510(k) K132075 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

PASSPORT M SERIES PATIENT MONITORING (INCLUDING MODELS PASSPORT 17M AND PASSPORT 12M)

ApplicantMindray North America, Mahwh NJ, US
DecisionSubstantially Equivalent, Apr 18, 2014
ReceivedJul 3, 2013
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K132075

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.