510(k) Report

FDA applicant

K & G Healthcare Ind., Inc.

Mchenry, IL3 decisions1981–19810 recalls

FDA records 3 decisions for K & G Healthcare Ind., Inc. (Mchenry, IL) in 1981: 3 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and KDQ (Bottle, Collection, Vacuum). 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, anesthesiology panel, where it files most

How often FDA has decided K & G Healthcare Ind., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for K & G Healthcare Ind., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — K & G Healthcare Ind., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • CAHFilter, Bacterial, Breathing-Circuit2decisions
  • KDQBottle, Collection, Vacuum1decision

What has FDA decided for it lately?

  • K812573Spirometer FilterK & G Healthcare Ind., Inc. · 1981
  • K812139Vacuum Suction FilterK & G Healthcare Ind., Inc. · 1981
  • K811546Nicholas II, Viral-Bacterial FilterK & G Healthcare Ind., Inc. · 1981

All 3 as K & G Healthcare Ind., Inc. →