K-number	K182519
Device name	Miha Bodytec II
Applicant	Miha Bodytec GmbH
Product code	NGX
Device class	Class II
Decision date	Jun 7, 2019
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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Miha Bodytec II

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