510(k) Report

FDA applicant

Eco-Rx, Inc.

Quebec City, Qc, CA1 decision2006–20060 recalls

FDA records 1 decision for Eco-Rx, Inc. (Quebec City, Qc, CA) in 2006: 1 510(k) clearance. All are in product code FRA (Purifier, Air, Ultraviolet, Medical). 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, general hospital panel, where it files most

How often FDA has decided Eco-Rx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eco-Rx, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eco-Rx, 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?

  • FRAPurifier, Air, Ultraviolet, Medical1decision

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.

  • K062716Eco-RX Air Purifier with UV Light, Model RX-400Eco-Rx, Inc. · 20062cite it

What has FDA decided for it lately?

  • K062716Eco-RX Air Purifier with UV Light, Model RX-400Eco-Rx, Inc. · 2006

The one decision as Eco-Rx, Inc. →