FDA applicant

Panasonic Co. Div. Matsu Elec. Corp. America

Mchenry, IL9 decisions1982–19860 recalls

FDA records 9 decisions for Panasonic Co. Div. Matsu Elec. Corp. America (Mchenry, IL) from 1982 to 1986: 9 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and ESD (Hearing Aid, Air-Conduction, Prescription). 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 Panasonic Co. Div. Matsu Elec. Corp. America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Panasonic Co. Div. Matsu Elec. Corp. America since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Panasonic Co. Div. Matsu Elec. Corp. America by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Panasonic Co. Div. Matsu Elec. Corp.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Panasonic”

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

Panasonic Healthcare Co., Ltd. 3 Panasonic Corporation (Panasonic) 2

Panasonic Co. Div. Matsu Elec. Corp. America

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Panasonic”