FDA applicant

The Healthcare Group Laboratories, Inc.

Mchenry, IL29 decisions1980–19850 recalls

FDA records 29 decisions for The Healthcare Group Laboratories, Inc. (Mchenry, IL) from 1980 to 1985: 29 510(k) clearances. Most are in product codes KOD (Catheter, Urological) and 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 The Healthcare Group Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Healthcare Group Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Healthcare Group Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?