Medical Device Manufacturer · US , Mchenry , IL

E.I. Dupont DE Nemours & Co., Inc. - FDA 510(k) Cleared Devices

253 submissions · 252 cleared · Since 1976
253
Total
252
Cleared
0
Denied

E.I. Dupont DE Nemours & Co., Inc. has 252 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 252 cleared submissions from 1976 to 1996.

Browse the FDA 510(k) cleared devices submitted by E.I. Dupont DE Nemours & Co., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - E.I. Dupont DE Nemours & Co., Inc.
253 devices
1-12 of 253

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