ClearanceBrief
510(k) K942347 ยท DQA Oximeter

NELLCOR SYMPHONY PULSE OXIMETER MODEL N-3000

ApplicantNellcor, Inc., Lenexa KS, US
DecisionSubstantially Equivalent, May 12, 1995
ReceivedMay 17, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942347

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.