Class Class II

aprevo® Digital Workflow (K222195)

K222195 2022-12-30 Traditional
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Description

aprevo® Digital Workflow by Carlsmed, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222195
Clearance Date2022-12-30
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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