ClearanceBrief
510(k) K822909 ยท DQA Oximeter

PULSE OXIMETER MODEL 100

ApplicantNellcor, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 1, 1982
ReceivedSep 30, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822909

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.