510(k) Report

FDA applicant

Noromed, Inc.

Seattle, WA2 decisions1992–19930 recalls

FDA records 2 decisions for Noromed, Inc. (Seattle, WA) from 1992 to 1993: 2 510(k) clearances. Most are in product codes HCC (Device, Biofeedback) and KQX (Goniometer, Ac-Powered). 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, neurology panel, where it files most

How often FDA has decided Noromed, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Noromed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Noromed, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • HCCDevice, Biofeedback1decision
  • KQXGoniometer, Ac-Powered1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K922838Norodyn 2000 ElectromyographNoromed, Inc. · 19931cites it

What has FDA decided for it lately?

  • K922838Norodyn 2000 ElectromyographNoromed, Inc. · 1993
  • K920690Norotrack 360 InclinometerNoromed, Inc. · 1992

All 2 as Noromed, Inc. →