Class Class II

VirtuOst (K220402)

K220402 2023-05-19 Traditional
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Description

VirtuOst by O.N. Diagnostics — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220402
Clearance Date2023-05-19
Clearance TypeTraditional
Product CodeKGI
Regulation Number892.1170

Categories

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