SHIAN JIA MEEI DIGATAL PWN TENS, MODEL YW-6000/UC-332/UC-330/ST-331— 510(k) K040311

Name: FDA 510(k) clearance K040311
Creator: U.S. Food and Drug Administration
Published: 2004-10-01

Substantially Equivalent

Shian Jia Meei Enterprise Co., Ltd.

FDA 510(k) clearance K040311 for SHIAN JIA MEEI DIGATAL PWN TENS, MODEL YW-6000/UC-332/UC-330/ST-331, Substantially Equivalent on 2004-10-01. Applicant: Shian Jia Meei Enterprise Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shian Jia Meei Enterprise Co., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2004-02-09
Decision date: 2004-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flagstaff, AZ, US

Download summary PDF View on FDA.gov ↗

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