E.I. Dupont DE Nemours & Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY, CRONEX RADIATION THERAPY CASSETTE, CRONEX RADIATION THERAPY VERIFICATION CASSETTE
253
Total
252
Cleared
0
Denied
FDA 510(k) Regulatory Record - E.I. Dupont DE Nemours & Co., Inc. Gastroenterology & Urology ✕
2 devices