510(k) Report

FDA applicant

American Thermal Instruments, Inc.

Mchenry, IL2 decisions1983–19840 recalls

FDA records 2 decisions for American Thermal Instruments, Inc. (Mchenry, IL) from 1983 to 1984: 2 510(k) clearances. Most are in product codes KPD (Strip, Temperature, Forehead, Liquid Crystal) and KXZ (System, Thermographic, Liquid Crystal, 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, general hospital panel, where it files most

How often FDA has decided American Thermal Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Thermal Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — American Thermal Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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