ClearanceBrief
510(k) K990082 ยท DQA Oximeter

EPIC SPO2 FINGER SENSOR, MODEL E403-09, E412-09 AND EPIC OXIMETER CABLE, MODEL E710-09

ApplicantEpic Medical Equipment Services, Inc., Plano TX, US
DecisionSubstantially Equivalent, Apr 9, 1999
ReceivedJan 11, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990082

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.