ClearanceBrief
510(k) K991823 ยท DQA Oximeter

N-395 PULSE OXIMETER, MODEL N-395

ApplicantNellcor Puritan Bennett, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Aug 25, 1999
ReceivedMay 28, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991823

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.