ClearanceBrief
510(k) K254209 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Radius VSM and Accessories

ApplicantMasimo Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Jun 4, 2026
ReceivedDec 29, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K254209

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.