ClearanceBrief
510(k) K081140 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

VISENSIA

ApplicantObs Medical, Carmel IN, US
DecisionSubstantially Equivalent, Jul 17, 2008
ReceivedApr 22, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081140

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.