ClearanceBrief
510(k) K991819 ยท DQA Oximeter

MAGNATEK 30

ApplicantMagna Advanced Technologies, Inc., Miami FL, US
DecisionSubstantially Equivalent, Aug 19, 1999
ReceivedMay 27, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991819

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.