FDA applicant

Euro-Electronics, Inc.

Miami, FL1 decision1985–19851 recall

FDA records 1 decision for Euro-Electronics, Inc. (Miami, FL) in 1985: 1 510(k) clearance. All are in product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 1 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 Euro-Electronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Euro-Electronics, Inc. since 2007.

Recalls per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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Euro-Electronics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?