EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR— 510(k) K071624

Name: FDA 510(k) clearance K071624
Creator: U.S. Food and Drug Administration
Published: 2007-11-27

Substantially Equivalent

Everlife Medical Equipment Co., Ltd.

FDA 510(k) clearance K071624 for EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR, Substantially Equivalent on 2007-11-27. Applicant: Everlife Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Everlife Medical Equipment Co., Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2007-06-14
Decision date: 2007-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu City, TW

Download summary PDF View on FDA.gov ↗

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