Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CP Relief Wand Rx - TENS/NMES

K-Number: K252236 · 2025-08-15

ApplicantN & C Holdings, LLC
Decision Date2025-08-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CP Relief Wand Rx - TENS/NMES is a medical device manufactured by N & C Holdings, LLC. It received FDA 510(k) clearance on 2025-08-15 under approval number K252236. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CP Relief Wand Rx - TENS/NMES?

CP Relief Wand Rx - TENS/NMES is a medical device that received FDA 510(k) clearance on 2025-08-15. It is manufactured by N & C Holdings, LLC. The 510(k) number is K252236.

When was CP Relief Wand Rx - TENS/NMES approved by the FDA?

CP Relief Wand Rx - TENS/NMES received FDA 510(k) clearance on 2025-08-15, under approval number K252236.

What company makes CP Relief Wand Rx - TENS/NMES?

CP Relief Wand Rx - TENS/NMES is manufactured by N & C Holdings, LLC.

What is the FDA product code for CP Relief Wand Rx - TENS/NMES?

The FDA product code for CP Relief Wand Rx - TENS/NMES is GZJ.

Related Devices (Code: GZJ)

K160246SimulCare II(TM)Xanacare Technologies, LLC K153704StriveDjo, LLC K152676FD TENS 2090, FD TENS 2095Fuji Dynamics , Ltd. K173233ReliefBand 1.5Reliefband Technologies K161091STIMPOD NMS460 Nerve StimulatorXavant Technology (Pty), Ltd. K162663WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605AWell-Life Healthcare Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑