FDA applicant

Geneva Laboratories, Inc.

Elkhorn, WI13 decisions1981–19880 recalls

FDA records 13 decisions for Geneva Laboratories, Inc. (Elkhorn, WI) from 1981 to 1988: 13 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and FPA (Set, Administration, Intravascular). 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 Geneva Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Geneva Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Geneva Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?