ClearanceBrief
510(k) K090172 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

STAR 55 MODEL 100

ApplicantLarsen & Toubro Limited, Schaumburg IL, US
DecisionSubstantially Equivalent, Jun 5, 2009
ReceivedJan 23, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090172

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.