510(k) Report

FDA applicant

C&H International

Houston, TX1 decision2002–20020 recalls

FDA records 1 decision for C&H International (Houston, TX) in 2002: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). Its devices cite 5 predicates, 0 of them its own earlier devices. 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 C&H International’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for C&H International since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — C&H International 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?

  • ILYLamp, Infrared, Therapeutic Heating1decision

Whose devices does it build on?

Its devices cite 5 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 5 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.

  • K020851TDP Heat Lamp or Infrared Heating Lamp, Models CQG-S1, CQG-111A/B, CQG-222A/B, CQG-270A/B, CQG-222DC&H International · 20025cite it

What has FDA decided for it lately?

  • K020851TDP Heat Lamp or Infrared Heating Lamp, Models CQG-S1, CQG-111A/B, CQG-222A/B, CQG-270A/B, CQG-222DC&H International · 2002

The one decision as C&H International →