FDA applicant

Thomson & Nielsen Electronics, Ltd.

Ottawa, Ontario, CA4 decisions2001–20040 recalls

FDA records 4 decisions for Thomson & Nielsen Electronics, Ltd. (Ottawa, Ontario, CA) from 2001 to 2004: 4 510(k) clearances. All are in product code IYE (Accelerator, Linear, Medical). 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 Thomson & Nielsen Electronics, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thomson & Nielsen Electronics, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Thomson & Nielsen Electronics, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Thomson”

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

Thomson-Cgr Medical Corp. 3 Thomson & Shelton Instrumentation Co, Inc. 1 Thomson-Csf Broadcast, Inc. 1

Thomson & Nielsen Electronics, Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Thomson”