ClearanceBrief
510(k) K840879 ยท LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

TOXO-G EIA DIAGNOSTIC KIT

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, May 21, 1984
ReceivedFeb 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840879

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.