Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)— 510(k) K222879

Name: FDA 510(k) clearance K222879
Creator: U.S. Food and Drug Administration
Published: 2023-01-24

Substantially Equivalent

Wuxi Jiajian Medical Instrument Co., Ltd.

FDA 510(k) clearance K222879 for Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1), Substantially Equivalent on 2023-01-24. Applicant: Wuxi Jiajian Medical Instrument Co., Ltd.. Device class: 2.

Clearance details

Applicant: Wuxi Jiajian Medical Instrument Co., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2022-09-22
Decision date: 2023-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wuxi, CN

Download summary PDF View on FDA.gov ↗

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K202893 — Transcutaneous Electrical Nerve Stimulator2021-06-18
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