Tens & Ems Device— 510(k) K223825

Name: FDA 510(k) clearance K223825
Creator: U.S. Food and Drug Administration
Published: 2023-05-09

Substantially Equivalent

Shenzhen Jian Feng Electronic Technology Co., Ltd.

FDA 510(k) clearance K223825 for Tens & Ems Device, Substantially Equivalent on 2023-05-09. Applicant: Shenzhen Jian Feng Electronic Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Jian Feng Electronic Technology Co., Ltd.
Product code: Code NUH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2022-12-21
Decision date: 2023-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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