K-number	K071666
Device name	SLENDERTONE ENERVIVE, MODEL 561
Applicant	Bio-Medical Research Corp.
Product code	NGX
Device class	Class II
Decision date	Mar 12, 2008
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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SLENDERTONE ENERVIVE, MODEL 561

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