FDA applicant

Panasonic Corporation (Panasonic)

Washington, DC2 decisions1999–19990 recalls

FDA records 2 decisions for Panasonic Corporation (Panasonic) (Washington, DC) in 1999: 2 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). Its devices cite 2 predicates, 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 Panasonic Corporation (Panasonic)’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Panasonic Corporation (Panasonic) since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Panasonic Corporation (Panasonic) by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Panasonic Corporation (Panasonic)’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 “Panasonic”

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

Panasonic Co. Div. Matsu Elec. Corp. America 9 Panasonic Healthcare Co., Ltd. 3

Panasonic Corporation (Panasonic)

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Panasonic”