ClearanceBrief
510(k) K070062 ยท LIO Device, Specimen Collection

COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USE

ApplicantDiesse Diagnostica Senese S.P.A., Hialeah FL, US
DecisionSubstantially Equivalent, Jul 30, 2007
ReceivedJan 5, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070062

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.