Needle Stimulator— 510(k) K202861

Name: FDA 510(k) clearance K202861
Creator: U.S. Food and Drug Administration
Published: 2021-08-27

Substantially Equivalent

Wuxi Jiajian Medical Instrument Co., Ltd.

FDA 510(k) clearance K202861 for Needle Stimulator, Substantially Equivalent on 2021-08-27. Applicant: Wuxi Jiajian Medical Instrument Co., Ltd.. Device class: Unclassified.

Clearance details

Applicant: Wuxi Jiajian Medical Instrument Co., Ltd.
Product code: Code BWK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2020-09-28
Decision date: 2021-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wuxi, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code BWK

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K200636 — AXUS ES-5 Electro-Acupuncture Device2021-02-03
K170391 — ANSiStim-PP2017-03-09
K152571 — Stivax2016-05-26

More clearances from Wuxi Jiajian Medical Instrument Co., Ltd.

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K231425 — Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)2024-03-27
K222879 — Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)2023-01-24
K202893 — Transcutaneous Electrical Nerve Stimulator2021-06-18
K192568 — Jiajian Self-Adhesive Electrode2021-02-03
K123958 — JIAJIAN POINTOSELECT DIGITAL2013-10-28

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