StimOnTM Pain Relief System (GM2439)

FDA 510(k) K213802 · Gimer Medical Co., Ltd.

Substantially Equivalent

510(k) numberK213802

Submission

Device name
StimOnTM Pain Relief System (GM2439)
Applicant
Gimer Medical Co., Ltd.
New Taipei City, TW
Received
December 6, 2021
Decision date
August 26, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5890
Specialty
Neurology

Other 510(k)s with product code GZJ

510(k)DeviceApplicantDecision
K252712STIMPOD NMS460 Nerve StimulatorGZJ · Traditional Algiamed Technologies USA, Inc.05/28/2026SE
K252767actiTENS miniGZJ · Traditional Sublimed01/16/2026SE
K252236CP Relief Wand Rx - TENS/NMESGZJ · Special N & C Holdings, LLC08/15/2025SE
K232441Unipro (K-UNIPRO-US)GZJ · Traditional Tenscare, Ltd.08/30/2024SE
K241228TENSWaveGZJ · Abbreviated Zynex Medical Officer08/27/2024SE
K233046Electrical Neuromuscular Stimulator, Cure TrioGZJ · Traditional Oriental Inspiration Limited04/19/2024SE
K222879Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)GZJ · Traditional Wuxi Jiajian Medical Instrument Co., Ltd.01/24/2023SE
K212618iRelieve Microcurrent Pain Relief SystemGZJ · Traditional Fast Track Technologies, Inc.09/14/2022SE
K220578Transcutaneous Electrical Nerve Stimulator (Model RJTENS-1)GZJ · Traditional Bozhou Rongjian Medical Appliance Co., Ltd.05/25/2022SE
K220503TENS device-EmeTerm 2, Model: YF-ZTY-E2GZJ · Traditional Wat Medical Technology, Inc.04/23/2022SE

Questions and answers

When was StimOnTM Pain Relief System (GM2439) cleared by the FDA?

StimOnTM Pain Relief System (GM2439) (K213802) received a 510(k) decision of Substantially Equivalent on August 26, 2022, 263 days after the submission was received.

What is the product code of K213802?

The FDA product code is GZJ – Stimulator, Nerve, Transcutaneous, For Pain Relief, a Class II (moderate risk) device regulated under 21 CFR 882.5890.