FDA applicant

Vee Gee Scientific, Inc.

Kirkland, WA6 decisions1994–19950 recalls

FDA records 6 decisions for Vee Gee Scientific, Inc. (Kirkland, WA) from 1994 to 1995: 6 510(k) clearances. All are in product code JRE (Refractometer For Clinical Use). 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 Vee Gee Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vee Gee Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vee Gee Scientific, Inc.

Which product codes does it file in?

What has FDA decided for it lately?