ClearanceBrief
510(k) K121863 ยท LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

VITEK 2 AST-ST CEFOTAXIME

ApplicantbioMerieux, Inc., Durham NC, US
DecisionSubstantially Equivalent, Aug 16, 2012
ReceivedJun 26, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121863

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.