ClearanceBrief
510(k) K113187 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

AVIVO MOBILE PATIENT MANAGEMENT

ApplicantCorventis, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Jan 4, 2012
ReceivedOct 31, 2011
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K113187

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.