ClearanceBrief
510(k) K910001 ยท DQA Oximeter

MODEL 8604-FO PULSE OXIMETER

ApplicantNonin Medical, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jul 18, 1991
ReceivedJan 2, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910001

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.