ClearanceBrief
510(k) K131876 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

M SERIES PATIENT MONITOR

ApplicantMid-Link Consulting Co, Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Feb 27, 2014
ReceivedJun 24, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K131876

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.