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FDA 510(k)

Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)

K-Number: K231425 · 2024-03-27

ApplicantWuxi Jiajian Medical Instrument Co., Ltd.
Decision Date2024-03-27
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) is the device name listed in this FDA 510(k) record. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2024-03-27 under 510(k) 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. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K231425.

When did Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) receive FDA 510(k) clearance?

Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1) received FDA 510(k) clearance on 2024-03-27, under 510(k) number K231425.

Who is the listed applicant for Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)?

The FDA 510(k) record lists Wuxi Jiajian Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT05348005Use of TENS Unit in the Management of Endometriosis PainCOMPLETEDNCT06411054The Efficacy of Acu-TENS as an Adjunct Analgesic During USG-MVARECRUITINGNCT06619418Assessment of Usability and Satisfaction With a Take-home Device Presenting Sound and Body Stimulation for Back PainRECRUITINGNCT07659314Post Operative Pain and Vagal StimulationNOT_YET_RECRUITINGNCT07680127TENS of Auricular Vagal Nerve for Radiation NecrosisNOT_YET_RECRUITINGNCT03148106Hand Rehabilitation Study for Stroke PatientsTERMINATED

Other records listing Wuxi Jiajian Medical Instrument Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)K222879Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)K202861Needle StimulatorK202893Transcutaneous Electrical Nerve StimulatorK192568Jiajian Self-Adhesive Electrode

Related Devices (Code: NUH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260412TENS 7000 Rechargeable 4 Channel (TENS 7000H)Shenzhen Dongdixin Technology Co., Ltd.K260425TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)Hivox Biotek, Inc.K253896TENS/EMS device (GUSE01)Globalcare Medical Technology Co., Ltd.K253305TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034)Shenzhen Jiantuo Electronics Co., Ltd.K253740TENS&EMS (HZ9151B, HZ9151C, HZ9151D)Hong Qiangxing (Shenzhen) Electronics LimitedK251958VEINOPLUS BackDynapulse Medical

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.

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