IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2— 510(k) K060975

Name: FDA 510(k) clearance K060975
Creator: U.S. Food and Drug Administration
Published: 2006-05-10

Substantially Equivalent

Theratech, Inc.

FDA 510(k) clearance K060975 for IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2, Substantially Equivalent on 2006-05-10. 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: 2006-04-10
Decision date: 2006-05-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Madison, TN, US

Download summary PDF View on FDA.gov ↗

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