510(k) Report

FDA applicant

Bowater Research, Inc.

Fox Lake, IL1 decision1993–19930 recalls

FDA records 1 decision for Bowater Research, Inc. (Fox Lake, IL) in 1993: 1 510(k) clearance. All are in product code IPF (Stimulator, Muscle, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Bowater Research, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bowater Research, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bowater Research, 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?

  • IPFStimulator, Muscle, Powered1decision

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.

  • K926410Ultratone 8+ & 20Bowater Research, Inc. · 19932cite it

What has FDA decided for it lately?

  • K926410Ultratone 8+ & 20Bowater Research, Inc. · 1993

The one decision as Bowater Research, Inc. →