ClearanceBrief
510(k) K121912 ยท DQA Oximeter

E1 EAR SENSORS

ApplicantMasimo Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Jul 24, 2012
ReceivedJul 2, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K121912

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.