ClearanceBrief
510(k) K954168 ยท DQA Oximeter

E100A PULSE OXIMETER FINGER SENSOR/PROBE

ApplicantEpic Medical Equipment Services, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Sep 12, 1996
ReceivedSep 5, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954168

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.