ClearanceBrief
510(k) K091899 ยท LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

VITEK 2 GRAM NEGATIVE MEROPENEM

ApplicantbioMerieux, Inc., Hazelwood MO, US
DecisionSubstantially Equivalent, Aug 14, 2009
ReceivedJun 25, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091899

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.