FDA applicant

X-Ray Accessory Corp.

Danielson, CT1 decision1997–19970 recalls

FDA records 1 decision for X-Ray Accessory Corp. (Danielson, CT) in 1997: 1 510(k) clearance. All are in product code IXJ (Grid, Radiographic). 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 Accessory Corp.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like X-Ray Accessory 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

X-Ray Accessory Corp.

Which product codes does it file in?

What has FDA decided for it lately?