510(k) Report

FDA applicant

Mwr Electronics Industrial Co.

Goodwood, Capetown, ZA1 decision1999–19990 recalls

FDA records 1 decision for Mwr Electronics Industrial Co. (Goodwood, Capetown, ZA) in 1999: 1 510(k) clearance. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Mwr Electronics Industrial Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mwr Electronics Industrial Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mwr Electronics Industrial Co.’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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