510(k) K252236

Device
CP Relief Wand Rx - TENS/NMES
Applicant
N & C Holdings, LLC
510(k) number
K252236
Product code
GZJ
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-15
Date received
2025-07-17
Regulation
882.5890
Classification name
Stimulator, Nerve, Transcutaneous, For Pain Relief
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Norm Schroeder
Address
1709 Honey Creek Rd. Jefferson City MO US 65101 65101

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code GZJ#

510(k), Device, Applicant table
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K213802StimOnTM Pain Relief System (GM2439)Gimer Medical Co., Ltd.2022-08-26
K220578Transcutaneous Electrical Nerve Stimulator (Model RJTENS-1)Bozhou Rongjian Medical Appliance Co., Ltd.2022-05-25
K220503TENS device-EmeTerm 2, Model: YF-ZTY-E2Wat Medical Technology, Inc.2022-04-23
K202893Transcutaneous Electrical Nerve StimulatorWuxi Jiajian Medical Instrument Co., Ltd.2021-06-18
K202186TrueRelief DeviceTruerelief2021-03-23
K210202BioWaveGO RXBiowave Corporation2021-02-24
K201458Scrambler Therapy Technology (Model ST-5A)Delta International Services & Logistics S.R.L2020-12-23
K202159actiTENSSublimed2020-12-22
K201431OGYILI TENS/NMES StimulatorGongguan Tutamen Metalwork Co., Ltd.2020-11-09