ClearanceBrief
510(k) K070791 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

PM SERIES PATIENT MONITORS, MODELS PM-9000 EXPRESS AND PM-8000 EXPRESS

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd., Great Neck NY, US
DecisionSubstantially Equivalent, Jun 26, 2007
ReceivedMar 22, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070791

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.