FDA applicant

Alleghany Intl. Medical Technology

St.Louis, MO3 decisions1985–19860 recalls

FDA records 3 decisions for Alleghany Intl. Medical Technology (St.Louis, MO) from 1985 to 1986: 3 510(k) clearances. All are in product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). 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, anesthesiology panel, where it files most

How often FDA has decided Alleghany Intl. Medical Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alleghany Intl. Medical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Alleghany Intl. Medical Technology by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Alleghany Intl. Medical Technology

Which product codes does it file in?

What has FDA decided for it lately?