ClearanceBrief
510(k) K071415 ยท DQA Oximeter

DIGITAL PULSE OXIMETER, MODEL 7500FO

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Aug 8, 2007
ReceivedMay 21, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071415

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.