ClearanceBrief
510(k) K873081 ยท DQA Oximeter

EDENTEC MULTI-CHANNEL RECORDER

ApplicantEdentec Corp., Eden Prairie MN, US
DecisionSubstantially Equivalent, Nov 17, 1987
ReceivedAug 5, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873081

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.