ClearanceBrief
510(k) K883558 ยท JSS Kit, Identification, Enterobacteriaceae

VITEK GRAM-NEGATIVE IDENTIFICATION CARD

ApplicantVitek Systems, Inc., Hazelwood MI, US
DecisionSubstantially Equivalent, Sep 16, 1988
ReceivedAug 19, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883558

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.