FDA applicant

Eureka X-Ray Tube Corp.

Mchenry, IL2 decisions1976–19900 recalls

FDA records 2 decisions for Eureka X-Ray Tube Corp. (Mchenry, IL) from 1976 to 1990: 2 510(k) clearances. Most are in product codes ITY (Assembly, Tube Housing, X-Ray, Diagnostic) and KPW (Device, Beam Limiting, 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 Eureka X-Ray Tube Corp.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Eureka X-Ray Tube Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Eureka”

FDA records each applicant name separately; these may or may not be the same firm.

Eureka Optics, Inc. 1 Eureka Laboratories, Inc. 1 Eureka AB 1

Eureka X-Ray Tube Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Eureka”