ClearanceBrief
510(k) K893240 ยท LJN Antibody Igm, If, Epstein-Barr Virus

BION EBV-M (VCA) TEST SYSTEM

ApplicantBion Ent., Ltd., Park Ridge IL, US
DecisionSubstantially Equivalent, Jul 14, 1989
ReceivedApr 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893240

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.