FDA applicant

Matsushita Electric Co.

Washington, DC2 decisions1991–19910 recalls

FDA records 2 decisions for Matsushita Electric Co. (Washington, DC) in 1991: 2 510(k) clearances. Most are in product codes JEQ (Toothbrush, Powered) and ISA (Massager, Therapeutic, Electric). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Matsushita Electric Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Matsushita Electric Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Matsushita”