ClearanceBrief
510(k) K841366 ยท KQJ System, Fibrinogen Determination

DIA FIBRIN

ApplicantDiatech, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 1, 1984
ReceivedApr 2, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841366

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.