510(k) Report

FDA applicant

International Distributors of Electronics For Medi

Benicia, CA1 decision2000–20000 recalls

FDA records 1 decision for International Distributors of Electronics For Medi (Benicia, CA) in 2000: 1 510(k) clearance. All are in product code ETY (Tester, Auditory Impedance). 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 International Distributors of Electronics For Medi’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for International Distributors of Electronics For Medi since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — International Distributors of Electronics For Medi 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?

  • ETYTester, Auditory Impedance1decision

Who builds on its devices?

Later devices cite its devices 4 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K994254Interacoustics AT235 Impedance AudiometerInternational Distributors of Electronics For Medi · 20004cite it

What has FDA decided for it lately?

  • K994254Interacoustics AT235 Impedance AudiometerInternational Distributors of Electronics For Medi · 2000

The one decision as International Distributors of Electronics For Medi →