510(k) Report

FDA applicant

Teltec Electronic Equipment AB

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Teltec Electronic Equipment AB (Mchenry, IL) in 1984: 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 Teltec Electronic Equipment AB’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teltec Electronic Equipment AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Teltec Electronic Equipment AB 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?

  • KLXElectroglottograph1decision

What has FDA decided for it lately?

  • K841832Glottal Frequency AnalyserTeltec Electronic Equipment AB · 1984

The one decision as Teltec Electronic Equipment AB →