K-number	K190038
Device name	Xbody Newave USA
Applicant	Xbody Hungary Kft.
Product code	NGX
Device class	Class II
Decision date	Apr 5, 2019
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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Xbody Newave USA

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