FDA applicant

Dufco Electronics, Inc.

Cambria, CA4 decisions1988–19880 recalls

FDA records 4 decisions for Dufco Electronics, Inc. (Cambria, CA) in 1988: 4 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Dufco Electronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dufco Electronics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dufco Electronics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Dufco Electronics, Inc.

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?