ClearanceBrief
510(k) K973970 ยท DQA Oximeter

SPO2 FINGER PROBES

ApplicantMedical Cables, Inc., Costa Mesa CA, US
DecisionSubstantially Equivalent, Oct 6, 1998
ReceivedOct 17, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973970

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.