Class Class II

Visionbody (K222386)

K222386 2023-02-24 Traditional
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Description

Visionbody by Vb Technologies AG — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222386
Clearance Date2023-02-24
Clearance TypeTraditional
Product CodeNGX
Regulation Number890.5850

Categories

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