FDA applicant

Electromedical Products, Inc.

Hawthorne, CA5 decisions1983–19920 recalls

FDA records 5 decisions for Electromedical Products, Inc. (Hawthorne, CA) from 1983 to 1992: 5 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and QJQ (Cranial Electrotherapy Stimulator To Treat…). 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 Electromedical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electromedical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Electromedical Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?