ClearanceBrief
510(k) K841020 ยท KQJ System, Fibrinogen Determination

FIBRINOGEN ASSAY KIT

ApplicantHelena Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, May 2, 1984
ReceivedMar 12, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841020

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.