ClearanceBrief
510(k) K122359 ยท LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

VITEK 2 STRPTOCOCCUS CEFTRIAXONE

ApplicantbioMerieux, Inc., Hazelwood MO, US
DecisionSubstantially Equivalent, Aug 28, 2012
ReceivedAug 3, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122359

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.