Class Class II

cCeLL – In vivo (K233391)

K233391 2024-08-21 Traditional
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Description

cCeLL - In vivo by VPIX Medical, Inc. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233391
Clearance Date2024-08-21
Clearance TypeTraditional
Product CodeGWG
Regulation Number882.1480

Categories

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