K-number	K060975
Device name	IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2
Applicant	Theratech, Inc.
Product code	LIH
Device class	Class II
Decision date	May 10, 2006
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2

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