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FDA 510(k)

Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)

K-Number: K231425 · 2024-03-27

Decision Date2024-03-27
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) is a medical device manufactured by Wuxi Jiajian Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2024-03-27 under approval number K231425. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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

Other Devices by Wuxi Jiajian Medical Instrument Co., Ltd.

Related Devices (Code: NUH)

Official Source

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