JOVS Electric Stimulation Beauty Device (JE2)— 510(k) K250227

Name: FDA 510(k) clearance K250227
Creator: U.S. Food and Drug Administration
Published: 2025-10-17

Substantially Equivalent

Shenzhen Qianyu Technology Co., Ltd.

FDA 510(k) clearance K250227 for JOVS Electric Stimulation Beauty Device (JE2), Substantially Equivalent on 2025-10-17. Applicant: Shenzhen Qianyu Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Qianyu Technology Co., Ltd.
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2025-01-27
Decision date: 2025-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen City, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.