ClearanceBrief
510(k) K890031 ยท LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

IMX TOXO IGG ANTIBODY ASSAY

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Jun 23, 1989
ReceivedJan 4, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890031

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.