510(k) Report

FDA applicant

Vocaltech C/O Hogan & Hartson

Washington, D.C., DC1 decision1987–19870 recalls

FDA records 1 decision for Vocaltech C/O Hogan & Hartson (Washington, D.C., DC) in 1987: 1 510(k) clearance. All are in product code KTH (Device, Anti-Stammering). 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 Vocaltech C/O Hogan & Hartson’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vocaltech C/O Hogan & Hartson since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vocaltech C/O Hogan & Hartson 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?

  • KTHDevice, Anti-Stammering1decision

What has FDA decided for it lately?

  • K871590Vocaltech Vocal Feedback DeviceVocaltech C/O Hogan & Hartson · 1987

The one decision as Vocaltech C/O Hogan & Hartson →