K-number	K003591
Device name	TENSCARE, MODEL TENS XL-2
Applicant	Tenscare, Ltd.
Product code	GZJ
Device class	Class II
Decision date	Feb 14, 2001
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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TENSCARE, MODEL TENS XL-2

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