FDA applicant

Murray Electronics

Hunt Valley, MD3 decisions1983–19990 recalls

FDA records 3 decisions for Murray Electronics (Hunt Valley, MD) from 1983 to 1999: 3 510(k) clearances. Most are in product codes NYN (Stimulator, Electrical, Transcutaneous, For…) and IPF (Stimulator, Muscle, Powered). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Murray Electronics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Murray Electronics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Murray”

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

Murray, Salk, Inc. 1

Murray Electronics

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?

Other applicant names beginning “Murray”