JIAJIAN POINTOSELECT DIGITAL— 510(k) K123958

Name: FDA 510(k) clearance K123958
Creator: U.S. Food and Drug Administration
Published: 2013-10-28

Substantially Equivalent

Wuxi Jiajian Medical Instrument Co., Ltd.

FDA 510(k) clearance K123958 for JIAJIAN POINTOSELECT DIGITAL, Substantially Equivalent on 2013-10-28. 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: 2012-12-21
Decision date: 2013-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shanghai, CN

Download summary PDF View on FDA.gov ↗

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