IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A— 510(k) K050847

Name: FDA 510(k) clearance K050847
Creator: U.S. Food and Drug Administration
Published: 2005-06-17

Substantially Equivalent

Theratech, Inc.

FDA 510(k) clearance K050847 for IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A, Substantially Equivalent on 2005-06-17. Applicant: Theratech, Inc.. Device class: 2.

Clearance details

Applicant: Theratech, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2005-04-04
Decision date: 2005-06-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Madison, TN, US

Download summary PDF View on FDA.gov ↗

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