FDA applicant

Armour Pharmaceutical Co.

Mchenry, IL7 decisions1984–19840 recalls

FDA records 7 decisions for Armour Pharmaceutical Co. (Mchenry, IL) in 1984: 7 510(k) clearances. Most are in product codes CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer)) and BZE (Heater, Breathing System W/Wo Controller (Not…). 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 Armour Pharmaceutical Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Armour Pharmaceutical Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Armour Pharmaceutical Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?