ClearanceBrief
510(k) K112843 ยท DQA Oximeter

PULSE OXIMETER

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Apr 19, 2012
ReceivedSep 29, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112843

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.