ClearanceBrief
510(k) K875363 ยท LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

SERODOT TOXOPLASMA IGG TEST KIT

ApplicantDisease Detection International, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Apr 21, 1988
ReceivedDec 31, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875363

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.