ClearanceBrief
510(k) K051439 ยท DQA Oximeter

LNOP BLUE OXIMETRY SENSOR

ApplicantMasimo Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Jul 15, 2005
ReceivedJun 2, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051439

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.