Class Class II

Clarus Viewer (K222757)

K222757 2023-02-24 Traditional
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Description

Clarus Viewer by Clarus Viewer Corporation — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222757
Clearance Date2023-02-24
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

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