ClearanceBrief
510(k) K833829 ยท LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

TOXOPLASMA GOND II IGG DIA TEST KIT

ApplicantLabsystems, Inc., Walker MI, US
DecisionSubstantially Equivalent, Apr 24, 1984
ReceivedNov 3, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833829

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.