ClearanceBrief
510(k) K083719 ยท NLF Oximeter, Reprocessed

LNCS OXIMETRY SENSORS

ApplicantMasimo Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Jul 30, 2009
ReceivedDec 15, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083719

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.