FDA applicant

Matsushita Electric Works, Ltd.

Great Neck, NY2 decisions2004–20050 recalls

FDA records 2 decisions for Matsushita Electric Works, Ltd. (Great Neck, NY) from 2004 to 2005: 2 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

How often FDA has decided Matsushita Electric Works, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Matsushita Electric Works, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Matsushita Electric Works, 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 “Matsushita”

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

Matsushita Electric Co. 2 Matsushita Electric Industrial Co., Ltd. 1 Matsushita Electric Corp. of America 1

Matsushita Electric Works, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Matsushita”