FDA applicant

Sanyo Electric, Inc.

Walker, MI3 decisions1982–19860 recalls

FDA records 3 decisions for Sanyo Electric, Inc. (Walker, MI) from 1982 to 1986: 3 510(k) clearances. Most are in product codes DRT (Monitor, Cardiac (Incl. Cardiotachometer &…) and DPS (Electrocardiograph). 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 Sanyo Electric, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sanyo Electric, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Sanyo”

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

Sanyo North America Corp. 1

Sanyo Electric, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sanyo”