ClearanceBrief
510(k) K913489 ยท DQA Oximeter

SIEMENS MICRO2 PULSE OXIMETER

ApplicantSiemens Medical Electronics, Danvers MA, US
DecisionSubstantially Equivalent, Oct 30, 1991
ReceivedAug 6, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913489

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.