FDA applicant

Msb,Uk

Marlborough,Wiltshire, GB1 decision1999–19990 recalls

FDA records 1 decision for Msb,Uk (Marlborough,Wiltshire, GB) in 1999: 1 510(k) clearance. All are in product code GXY (Electrode, Cutaneous). 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 Msb,Uk’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Msb,Uk since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Msb,Uk’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

Msb,Uk

Which product codes does it file in?

What has FDA decided for it lately?