ClearanceBrief
510(k) K842759 ยท LOS

MODEL 503FB

ApplicantAtrix, Portland OR, US
DecisionSubstantially Equivalent, Jan 18, 1985
ReceivedJul 16, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842759

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.