ClearanceBrief
510(k) K071285 ยท DQA Oximeter

DIGITAL PULSE OXIMETER, MODEL 7500

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Jul 12, 2007
ReceivedMay 7, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071285

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.