JIAJIAN TENS— 510(k) K112288

Name: FDA 510(k) clearance K112288
Creator: U.S. Food and Drug Administration
Published: 2012-05-02

Substantially Equivalent

Wuxi Jiajian Medical Instrument Co., Ltd.

FDA 510(k) clearance K112288 for JIAJIAN TENS, Substantially Equivalent on 2012-05-02. 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: 2011-08-09
Decision date: 2012-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shanghai, CN

Download summary PDF View on FDA.gov ↗

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