FDA applicant

Manfred Sauer Corp.

Mchenry, IL4 decisions1981–19810 recalls

FDA records 4 decisions for Manfred Sauer Corp. (Mchenry, IL) in 1981: 4 510(k) clearances. All are in product code KNX (Collector, Urine, (And Accessories) For…). 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 Manfred Sauer Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Manfred Sauer Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Manfred Sauer Corp.

Which product codes does it file in?

What has FDA decided for it lately?