ClearanceBrief
510(k) K923593 ยท KQJ System, Fibrinogen Determination

HEMOCHRON/FACTOR VI FIBRINOGEN ASSAY AND CONT PLAS

ApplicantInternational Technidyne Corp., Edison NJ, US
DecisionSubstantially Equivalent, Sep 22, 1992
ReceivedJul 20, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923593

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.