Class Class II

XBody Go USA, XBody Pro USA (K221200)

K221200 2023-01-31 Traditional
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Description

XBody Go USA, XBody Pro USA by Xbody Hungary Kft. — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221200
Clearance Date2023-01-31
Clearance TypeTraditional
Product CodeNGX
Regulation Number890.5850

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