Care Stim

FDA 510(k) K022417 · Care Rehab and Orthopaedic

Substantially Equivalent

510(k) numberK022417

Submission

Device name
Care Stim
Applicant
Care Rehab and Orthopaedic
Mclean, VA, US
Received
July 24, 2002
Decision date
April 10, 2003
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
K213802StimOnTM Pain Relief System (GM2439)GZJ · Traditional Gimer Medical Co., Ltd.08/26/2022SE
K220578Transcutaneous Electrical Nerve Stimulator (Model RJTENS-1)GZJ · Traditional Bozhou Rongjian Medical Appliance Co., Ltd.05/25/2022SE

More from Bozhou Rongjian Medical Appliance Co., Ltd.

510(k)DeviceDecision
K023036Care EtsIPF · Traditional 06/19/2003SE
K020637Select StimIPF · Traditional 05/28/2002SE

Questions and answers

When was Care Stim cleared by the FDA?

Care Stim (K022417) received a 510(k) decision of Substantially Equivalent on April 10, 2003, 260 days after the submission was received.

What is the product code of K022417?

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