ClearanceBrief
510(k) K895567 ยท LFT Fluorescent Immunoassay, Primidone

PRIMIDONE (FPIA) KIT

ApplicantTudor Laboratories, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Oct 20, 1989
ReceivedSep 6, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895567

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.