510(k) Report

FDA applicant

Paraproducts, Inc.

Itasca, IL1 decision2000–20000 recalls

FDA records 1 decision for Paraproducts, Inc. (Itasca, IL) in 2000: 1 510(k) clearance. All are in product code BTR (Tube, Tracheal (W/Wo Connector)). 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 Paraproducts, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paraproducts, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Paraproducts, 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?

  • BTRTube, Tracheal (W/Wo Connector)1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K000045PositubeParaproducts, Inc. · 20002cite it

What has FDA decided for it lately?

  • K000045PositubeParaproducts, Inc. · 2000

The one decision as Paraproducts, Inc. →