FDA applicant

Tes Electrical Electronic Corp.

Taipei, Taiwan 300, CN1 decision1999–19990 recalls

FDA records 1 decision for Tes Electrical Electronic Corp. (Taipei, Taiwan 300, CN) in 1999: 1 510(k) clearance. All are in product code MWJ (Electrocardiograph, Ambulatory (Without…). 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 Tes Electrical Electronic Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tes Electrical Electronic Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tes Electrical Electronic Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Tes Electrical Electronic Corp.

Which product codes does it file in?

What has FDA decided for it lately?