Class Class II

Clarius AI (K222406)

K222406 2023-01-23 Traditional
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Description

Clarius AI by Clarius Mobile Health Corp. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222406
Clearance Date2023-01-23
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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