510(k) Report

FDA applicant

Posey Co.

Elk Grove Village, IL2 decisions1987–19910 recalls

FDA records 2 decisions for Posey Co. (Elk Grove Village, IL) from 1987 to 1991: 2 510(k) clearances. Most are in product codes BTO (Tube, Tracheostomy (W/Wo Connector)) and BSK (Cuff, Tracheal Tube, Inflatable). 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 Posey Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Posey Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Posey Co. 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?

  • BTOTube, Tracheostomy (W/Wo Connector)1decision
  • BSKCuff, Tracheal Tube, Inflatable1decision

Who builds on its devices?

Later devices cite its devices 6 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K912723Posey CufflatorPosey Co. · 19916cite it

What has FDA decided for it lately?

  • K912723Posey CufflatorPosey Co. · 1991
  • K874742QuicktrachPosey Co. · 1987

All 2 as Posey Co. →