FDA applicant

X-Ray Tube Corp.

Walker, MI3 decisions1983–19840 recalls

FDA records 3 decisions for X-Ray Tube Corp. (Walker, MI) from 1983 to 1984: 3 510(k) clearances. All are in product code ITY (Assembly, Tube Housing, X-Ray, Diagnostic). 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 X-Ray Tube Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for X-Ray Tube Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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X-Ray Tube Corp.

Which product codes does it file in?

What has FDA decided for it lately?