ClearanceBrief
510(k) K030722 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

ENVOY PATIENT MONITOR

ApplicantMennen Medical, Inc., Rehovot, IL
DecisionSubstantially Equivalent, Feb 26, 2004
ReceivedMar 7, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030722

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.