K-number	K210174
Device name	BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set
Applicant	Bemer Int AG
Product code	NGX
Device class	Class II
Decision date	Feb 4, 2021
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set

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