FDA applicant

Matsushita Electric Industrial Co., Ltd.

Rockville, MD1 decision2001–20011 recall

FDA records 1 decision for Matsushita Electric Industrial Co., Ltd. (Rockville, MD) in 2001: 1 510(k) clearance. All are in product code MWI (Monitor, Physiological, Patient (Without…). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Matsushita Electric Industrial Co., Ltd. since 2007.

Recalls per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Matsushita Electric Industrial Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Matsushita Electric Industrial Co., Ltd.’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

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 Co. 2 Matsushita Electric Corp. of America 1

Matsushita Electric Industrial Co., 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?

What has been recalled?

Other applicant names beginning “Matsushita”