ClearanceBrief
510(k) K123021 ยท LJN Antibody Igm, If, Epstein-Barr Virus

BIOPLEX 2200 EBV IGM KIT

ApplicantBio-Rad Laboratories, Benicia CA, US
DecisionSubstantially Equivalent, Nov 2, 2012
ReceivedSep 27, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123021

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.