510(k) Report

FDA applicant

Jeol

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Jeol (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code IYM (System, Telethermographic, Infrared). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Jeol since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jeol 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?

  • IYMSystem, Telethermographic, Infrared1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K823041Jeol Model #JTG-500MJeol · 19821cites it

What has FDA decided for it lately?

  • K823041Jeol Model #JTG-500MJeol · 1982

The one decision as Jeol →