Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)
K-Number: K222879 · 2023-01-24
Device Summary
Frequently Asked Questions
What is the Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)?
Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1) is a medical device that received FDA 510(k) clearance on 2023-01-24. It is manufactured by Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K222879.
When was Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1) approved by the FDA?
Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1) received FDA 510(k) clearance on 2023-01-24, under approval number K222879.
What company makes Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)?
Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1) is manufactured by Wuxi Jiajian Medical Instrument Co., Ltd..
What is the FDA product code for Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)?
The FDA product code for Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1) is GZJ.
Related Clinical Trials
Other Devices by Wuxi Jiajian Medical Instrument Co., Ltd.
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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.