FDA applicant

Fisons Corp.

Mchenry, IL3 decisions1977–19950 recalls

FDA records 3 decisions for Fisons Corp. (Mchenry, IL) from 1977 to 1995: 3 510(k) clearances. Most are in product codes FLG (Cleaner, Ultrasonic, Medical Instrument) and CAF (Nebulizer (Direct Patient Interface)). 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 Fisons Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fisons Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Fisons Corp.

Which product codes does it file in?

What has FDA decided for it lately?