Medical Device Manufacturer · US , Wilmington , DE

The DU Pont Co. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1988

Total

Cleared

Denied

The DU Pont Co. has 13 FDA 510(k) cleared medical devices. Based in Wilmington, US.

Historical record: 13 cleared submissions from 1988 to 1995. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by The DU Pont Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - The DU Pont Co.

13 devices

1-13 of 13

Cleared Oct 07, 1995

CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGING

K953475 · LMC

Radiology · 75d

Cleared Oct 07, 1995

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING

K953477 · LMC

Radiology · 75d

Cleared Jul 13, 1995

CRONEX LOW ABSORPTION CASSETTE

K952891 · IXA

Radiology · 20d

Cleared Mar 10, 1995

DUPONT ACA VANCOMYCIN (VANC) METHOD

LABELING CHANGE - VIASPAN(TM) (BELZER UW)

K900492 · KDL

Gastroenterology & Urology · 46d

Cleared Feb 17, 1989

ACA THYROXINE (T4 E) METHOD

K885258 · KLI

Chemistry · 56d

Cleared Feb 17, 1989

ACA THYRONINE UPTAKE (TU E) METHOD

K885259 · KHQ

Chemistry · 56d

Cleared Jan 27, 1989

ANALYST THYROXINE (T4) ROTOR

K884700 · KLI

Chemistry · 79d

Cleared Jan 24, 1989

DU PONT ANALYST THYROID ROTOR

K884169 · CEL

Chemistry · 112d

Cleared Nov 29, 1988

ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.

K884168 · JIS

Chemistry · 56d

Cleared Nov 16, 1988

ANALYST THEOPHYLLINE CALIBRATOR

K884170 · DLJ

Toxicology · 56d

Cleared Oct 31, 1988

ANALYST THEOPHYLLINE ROTOR

K884002 · KLS

Toxicology · 40d

The DU Pont Co. - FDA 510(k) Cleared Devices

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