ClearanceBrief
510(k) K884249 ยท LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

MODIFIED DDI SEROCARD TOXOPLASMA IGG TEST KIT

ApplicantDisease Detection International, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Apr 10, 1989
ReceivedOct 11, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884249

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.