TUNG FU AIRMATE TENS, VITALITY MODE, TF-DT001— 510(k) K042107

Name: FDA 510(k) clearance K042107
Creator: U.S. Food and Drug Administration
Published: 2005-03-09

Substantially Equivalent

Tung FU Electric Co., Ltd.

FDA 510(k) clearance K042107 for TUNG FU AIRMATE TENS, VITALITY MODE, TF-DT001, Substantially Equivalent on 2005-03-09. Applicant: Tung FU Electric Co., Ltd.. Device class: 2.

Clearance details

Applicant: Tung FU Electric Co., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2004-08-04
Decision date: 2005-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin Chu City, TW

Download summary PDF View on FDA.gov ↗

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