FDA applicant

Ab Medett Produkter

Mchenry, IL3 decisions1979–19790 recalls

FDA records 3 decisions for Ab Medett Produkter (Mchenry, IL) in 1979: 3 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and KNK (Acid, Uric, Uricase (Colorimetric)). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Ab Medett Produkter’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ab Medett Produkter since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ab Medett Produkter

Which product codes does it file in?

What has FDA decided for it lately?