ClearanceBrief
510(k) K852519 ยท JCO Bothrops Atrox Reagent

DUPONT ACA FIBRIN DEGRADATION PROD CLOTTING TUBE

ApplicantE.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US
DecisionSubstantially Equivalent, Aug 12, 1985
ReceivedJun 17, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852519

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.