ClearanceBrief
510(k) K220805 ยท LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

VITEK 2 AST-Gram Positive Cefoxitin Screen

ApplicantbioMerieux, Inc., Hazelwood MO, US
DecisionSubstantially Equivalent, Oct 13, 2022
ReceivedMar 18, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220805

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.