ClearanceBrief
510(k) K982907 ยท DQA Oximeter

MAGNATEK 40

ApplicantMagna Advanced Technologies, Inc., Miami FL, US
DecisionSubstantially Equivalent, Oct 2, 1998
ReceivedAug 18, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982907

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.