FDA applicant

The DU Pont Co.

Wilmington, DE13 decisions1988–19950 recalls

FDA records 13 decisions for The DU Pont Co. (Wilmington, DE) from 1988 to 1995: 13 510(k) clearances. Most are in product codes LMC (Camera, Multi Format, Radiological) and KLI (Enzyme Immunoassay, Non-Radiolabeled, Total…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided The DU Pont Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The DU Pont Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The DU Pont Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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The DU Pont Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?