EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507— 510(k) K070890

Name: FDA 510(k) clearance K070890
Creator: U.S. Food and Drug Administration
Published: 2007-06-29

Substantially Equivalent

Everlife Medical Equipment Co., Ltd.

FDA 510(k) clearance K070890 for EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507, Substantially Equivalent on 2007-06-29. Applicant: Everlife Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Everlife Medical Equipment Co., Ltd.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2007-03-30
Decision date: 2007-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu City, TW

Download summary PDF View on FDA.gov ↗

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