ClearanceBrief
510(k) K041982 ยท LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

VITEK 2 GRAM NEGATIVE ERTAPENEM

ApplicantbioMerieux, Inc., Hazelwood MO, US
DecisionSubstantially Equivalent, Sep 14, 2004
ReceivedJul 23, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041982

DateFirm and productCodeLinked 510(k)
Jan 4, 2023Biomerieux Inc
VITEK 2 REAGENT AST-GN81 TEST KIT 20 CARDS, CATALOG 413438
Open, Classified
LONNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.