ClearanceBrief
510(k) K830364 ยท JSX Kit, Identification, Neisseria Gonorrhoeae

NEISSERIA IDENTIFICATION DISCS

ApplicantOxoid U.S.A., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 8, 1983
ReceivedFeb 4, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830364

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.