FDA applicant

General X-Ray, Inc.

Mchenry, IL14 decisions1978–19800 recalls

FDA records 14 decisions for General X-Ray, Inc. (Mchenry, IL) from 1978 to 1980: 14 510(k) clearances. Most are in product codes IZL (System, X-Ray, Mobile) and KPQ (System, Simulation, Radiation Therapy). 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, radiology panel, where it files most

How often FDA has decided General X-Ray, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for General X-Ray, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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General X-Ray, Inc.

Which product codes does it file in?

What has FDA decided for it lately?