ClearanceBrief
510(k) K061442 ยท DQA Oximeter

PULSE OXIMETER, MODEL PM-50

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd., Great Neck NY, US
DecisionSubstantially Equivalent, Sep 5, 2006
ReceivedMay 24, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K061442

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.