ClearanceBrief
510(k) K801926 ยท KQJ System, Fibrinogen Determination

SIGMA PROCEDURE #880 FIBRINOGIN/PLASMA

ApplicantSigma Chemical Co., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 9, 1980
ReceivedAug 12, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801926

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.