CP Relief Wand Rx - TENS/NMES— 510(k) K252236

Name: FDA 510(k) clearance K252236
Creator: U.S. Food and Drug Administration
Published: 2025-08-15

Substantially Equivalent

N & C Holdings, LLC

FDA 510(k) clearance K252236 for CP Relief Wand Rx - TENS/NMES, Substantially Equivalent on 2025-08-15. Applicant: N & C Holdings, LLC. Device class: 2.

Clearance details

Applicant: N & C Holdings, LLC
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2025-07-17
Decision date: 2025-08-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Jefferson City, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZJ

view all

K252712 — STIMPOD NMS460 Nerve Stimulator2026-05-28
K252767 — actiTENS mini2026-01-16
K232441 — Unipro (K-UNIPRO-US)2024-08-30
K241228 — TENSWave2024-08-27
K233046 — Electrical Neuromuscular Stimulator, Cure Trio2024-04-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.