ClearanceBrief
510(k) K081285 ยท DQA Oximeter

FINGER PULSE OXIMETER, MODEL 9560

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Jun 5, 2008
ReceivedMay 6, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081285

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.