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

FDA 510(k) Regulatory Record - E.I. Dupont DE Nemours & Co., Inc. Radiology ✕

26 devices

1-12 of 26

Cleared Sep 06, 1995

CRONEX RADIATION THERAPY CASSETTE

Radiology · 27d

Cleared Sep 06, 1995

CRONEX RADIATION THERAPY VERIFICATION CASSETTE

Radiology · 27d

Cleared Jun 08, 1993

DU PONT MV DARKROOM CASSETTE

Radiology · 98d

Cleared Jun 08, 1993

MICROVISION FAST DETAIL INTENSIFYING SCREEN

Radiology · 88d

Cleared Dec 07, 1992

DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II)

Radiology · 89d

Cleared Nov 09, 1992

DU PONT LINX HD-25 LASR IMAGER

Radiology · 138d

Cleared Sep 11, 1992

DU PONT COMPACT DAYLIGHT SYSTEM 2000

Radiology · 107d

Cleared May 28, 1992

ULTRA-VISION RAPID INTENSIFYING SCREEN

Radiology · 134d

Cleared May 28, 1992

ULTRA-VISION DETAIL INTENSIFYING SCREEN

Radiology · 134d

Cleared May 27, 1992

ULTRA-VISION FAST DETAIL INTENSIFYING SCREEN

Radiology · 133d

Cleared May 15, 1990

DU PONT LINX LASER IMAGER W/THE LINX NETWORKING

Radiology · 76d

Cleared Feb 26, 1990

DU PONT MAMMOGRAPHY CASSETTE

Radiology · 18d