FDA product code · Neurology

Stimulator, Nerve, Electrical, Transcutaneous, With Limited Output, For Pain Relief

Name: FDA decisions, review times, recalls and adverse event reports for product code NYW
Creator: 510(k) Report

NYWClass II21 CFR 882.5890510(k) required0 decisions0 recalls

0 FDA decisions. No recall names this code.

Nerve stimulation for relief of pain

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, neurology panel

Twenty years of NYW at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

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

Planning a device in NYW? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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