Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)
K-Number: K231425 · 2024-03-27
Device Summary
Frequently Asked Questions
What is the Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)?
Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) is a medical device that received FDA 510(k) clearance on 2024-03-27. It is manufactured by Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K231425.
When was Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) approved by the FDA?
Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) received FDA 510(k) clearance on 2024-03-27, under approval number K231425.
What company makes Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)?
Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) is manufactured by Wuxi Jiajian Medical Instrument Co., Ltd..
What is the FDA product code for Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)?
The FDA product code for Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) is NUH.
Related Clinical Trials
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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.