ClearanceBrief
510(k) K860051 ยท DQA Oximeter

MODEL 8604 OXYGEN/PULSE MONITOR

ApplicantNonin Medical, Inc., White Bear Lake MN, US
DecisionSubstantially Equivalent, Jun 5, 1986
ReceivedJan 6, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860051

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.