K-number	K151834
Device name	BEMER Classic Set, BEMER Pro-Set
Applicant	Bemer Int AG
Product code	NGX
Device class	Class II
Decision date	Feb 22, 2017
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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BEMER Classic Set, BEMER Pro-Set

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