510(k) Report

FDA applicant

Yamasa Shoy Co., Ltd.

Chuoku, Tokyo 103 Japan, JP2 decisions1989–19890 recalls

FDA records 2 decisions for Yamasa Shoy Co., Ltd. (Chuoku, Tokyo 103 Japan, JP) in 1989: 2 510(k) clearances. All are in product code CDF (Acid, Vanilmandelic, Diazo…). 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, clinical chemistry panel, where it files most

How often FDA has decided Yamasa Shoy Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Yamasa Shoy Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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