ClearanceBrief
510(k) K921045 ยท JXA Kit, Screening, Urine

DIASLIDE URINE CULTURING DEVICE

ApplicantSavyon Diagnostics , Ltd., Ashdod, IL
DecisionSubstantially Equivalent, Sep 28, 1992
ReceivedMar 4, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921045

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.