FDA applicant

Ms. Kate Teaney

Walker, MI1 decision1982–19820 recalls

FDA records 1 decision for Ms. Kate Teaney (Walker, MI) in 1982: 1 510(k) clearance. All are in product code KLX (Electroglottograph). 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 Ms. Kate Teaney’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ms. Kate Teaney since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ms. Kate Teaney by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Ms. Kate Teaney

Which product codes does it file in?

What has FDA decided for it lately?