Class Class II

LVivo IQS (K222970)

K222970 2023-02-01 Traditional
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Description

LVivo IQS by Dia Imaging Analysis, Ltd. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222970
Clearance Date2023-02-01
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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