FDA applicant

Antares Technical Associates, Inc.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Antares Technical Associates, Inc. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code ETK (Tube, Toynbee Diagnostic). 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, ear, nose and throat panel, where it files most

How often FDA has decided Antares Technical Associates, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Antares Technical Associates, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Antares Technical Associates, Inc.

Which product codes does it file in?

What has FDA decided for it lately?