K-number	K203513
Device name	SLENDERTONE Evolve Abs, Type 735
Applicant	Bio-Medical Research, Ltd.
Product code	NGX
Device class	Class II
Decision date	Feb 10, 2021
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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SLENDERTONE Evolve Abs, Type 735

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