K-number	K221200
Device name	XBody Go USA, XBody Pro USA
Applicant	Xbody Hungary Kft.
Product code	NGX
Device class	Class II
Decision date	Jan 31, 2023
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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XBody Go USA, XBody Pro USA

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