K-number	K010335
Device name	SLENDERTONE FLEX, MODEL, 512
Applicant	Bio-Medical Research, Ltd.
Product code	NGX
Device class	Class II
Decision date	Sep 27, 2001
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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SLENDERTONE FLEX, MODEL, 512

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