FDA applicant

Hudson Kendale Assoc., Inc.

Mchenry, IL1 decision1979–19790 recalls

FDA records 1 decision for Hudson Kendale Assoc., Inc. (Mchenry, IL) in 1979: 1 510(k) clearance. All are in product code KPL (Colonic Irrigation System). 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 Hudson Kendale Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hudson Kendale Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Hudson”

FDA records each applicant name separately; these may or may not be the same firm.

Hudson Oxygen Therapy Sales Co. 33 Hudson Respiratory Care, Inc. 15 Hudson Extrusions, Inc. 2 Hudson Diagnostic Imaging, LLC 2 Hudson Rcj AB 1

Hudson Kendale Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hudson”