IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND— 510(k) K024100

Name: FDA 510(k) clearance K024100
Creator: U.S. Food and Drug Administration
Published: 2003-02-25

Substantially Equivalent

Theratech, Inc.

FDA 510(k) clearance K024100 for IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND, Substantially Equivalent on 2003-02-25. Applicant: Theratech, Inc.. Device class: 2.

Clearance details

Applicant: Theratech, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-12-12
Decision date: 2003-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung, TW

Download summary PDF View on FDA.gov ↗

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