510(k) K951441

DUPONT ACA DIGOXIN (DGN A) METHOD by E.I. Dupont DE Nemours & Co., Inc. — Product Code KXT

K951441 is an FDA 510(k) premarket notification submitted by E.I. Dupont DE Nemours & Co., Inc. for the device "DUPONT ACA DIGOXIN (DGN A) METHOD". The FDA issued a decision of Substantially Equivalent on June 1, 1995. The device falls under product code KXT (Enzyme Immunoassay, Digoxin), a Class II device regulated under 21 CFR 862.3320. E.I. Dupont DE Nemours & Co., Inc. has at least 10 other 510(k) clearances on record.