ClearanceBrief
510(k) K132077 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

PATIENT MONITOR

ApplicantAdvanced Instrumentations, Inc., Hialeah FL, US
DecisionSubstantially Equivalent, Apr 23, 2014
ReceivedJul 5, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132077

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.