ClearanceBrief
510(k) K960759 ยท JSX Kit, Identification, Neisseria Gonorrhoeae

GONOPOX TEST KIT

ApplicantMedtex Laboratories, Inc., Seattle WA, US
DecisionSubstantially Equivalent, Sep 18, 1996
ReceivedFeb 26, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960759

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.