ClearanceBrief
510(k) K221879 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Patient Monitor, models LM-8, LM-10, LM-12 and LM-15

ApplicantCaf Medical Solutions, Inc., Hockley TX, US
DecisionSubstantially Equivalent, Aug 10, 2022
ReceivedJun 28, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221879

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.