Powered Muscle Stimulator (Model name:MagGraver F200)— 510(k) K222875

Name: FDA 510(k) clearance K222875
Creator: U.S. Food and Drug Administration
Published: 2023-03-09

Substantially Equivalent

Nanjing Vishee Medical Technology Co., Ltd.

FDA 510(k) clearance K222875 for Powered Muscle Stimulator (Model name:MagGraver F200), Substantially Equivalent on 2023-03-09. Applicant: Nanjing Vishee Medical Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Nanjing Vishee Medical Technology Co., Ltd.
Product code: Code NGX
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2022-09-22
Decision date: 2023-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nanjing, 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.