FINESUN EMS STIMULATOR— 510(k) K020684

Name: FDA 510(k) clearance K020684
Creator: U.S. Food and Drug Administration
Published: 2002-05-23

Substantially Equivalent

Finesun Worldwide Intl. Co., Ltd.

FDA 510(k) clearance K020684 for FINESUN EMS STIMULATOR, Substantially Equivalent on 2002-05-23. Applicant: Finesun Worldwide Intl. Co., Ltd.. Device class: 2.

Clearance details

Applicant: Finesun Worldwide Intl. Co., Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2002-03-04
Decision date: 2002-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu, TW

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