FDA applicant

U. S. A. Imaging Corp.

Mchenry, IL3 decisions1982–19820 recalls

FDA records 3 decisions for U. S. A. Imaging Corp. (Mchenry, IL) in 1982: 3 510(k) clearances. All are in product code IYO (System, Imaging, Pulsed Echo, Ultrasonic). 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 U. S. A. Imaging Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for U. S. A. Imaging Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — U. S. A. Imaging Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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U. S. A. Imaging Corp.

Which product codes does it file in?

What has FDA decided for it lately?