510(k) Report

FDA applicant

Mercury Electronics (Scot), Ltd.

Glasgow 577 6nu U.K., GB1 decision1992–19920 recalls

FDA records 1 decision for Mercury Electronics (Scot), Ltd. (Glasgow 577 6nu U.K., GB) in 1992: 1 510(k) clearance. All are in product code EWO (Audiometer). 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 Mercury Electronics (Scot), Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mercury Electronics (Scot), Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mercury Electronics (Scot), Ltd. 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?

  • EWOAudiometer1decision

What has FDA decided for it lately?

  • K914232Asra, Screening AudiometerMercury Electronics (Scot), Ltd. · 1992

The one decision as Mercury Electronics (Scot), Ltd. →

Other applicant names beginning “Mercury”

FDA records each applicant name separately; these may or may not be the same firm.

Mercury Medical 16Mercury Enterprises, Inc. 3Mercury Computer Systems, Inc. 2Mercury Ent., Inc. D/B/A Mercury Medical 1Mercury Enterprizes Dba Mercury Medical 1