FDA applicant

American Viggo

Mchenry, IL10 decisions1976–19770 recalls

FDA records 10 decisions for American Viggo (Mchenry, IL) from 1976 to 1977: 10 510(k) clearances. Most are in product codes FMG (Stopcock, I.V. Set) and FOZ (Catheter, Intravascular, Therapeutic…). 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, general hospital panel, where it files most

How often FDA has decided American Viggo’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Viggo since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Viggo

Which product codes does it file in?

What has FDA decided for it lately?