ClearanceBrief
510(k) K972535 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

MAGLIFE C

ApplicantOdam, North Attleboro MA, US
DecisionSubstantially Equivalent, Jan 13, 1998
ReceivedJul 8, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972535

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.