FDA applicant

Autoject Systems, Inc.

Oak Dale, IL4 decisions1986–19950 recalls

FDA records 4 decisions for Autoject Systems, Inc. (Oak Dale, IL) from 1986 to 1995: 4 510(k) clearances. Most are in product codes HCC (Device, Biofeedback) and KZE (Injector, Fluid, Non-Electrically 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Autoject Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Autoject Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?