ClearanceBrief
510(k) K051107 ยท DQA Oximeter

ONYX II FINGER PULSE OXIMETER, MODEL 9550

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Jun 1, 2005
ReceivedMay 2, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K051107

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.