ClearanceBrief
510(k) K023044 ยท DQA Oximeter

MODEL 9600, AVANT PULSE OXIMETER

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Jul 23, 2003
ReceivedSep 12, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023044

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.