Class Class II

CarnaLife Holo (K221870)

K221870 2023-05-01 Traditional
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Description

CarnaLife Holo by Medapp S.A. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221870
Clearance Date2023-05-01
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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