Class Class II

Ceribell Delirium Monitor System (K251936)

K251936 2025-12-08 Traditional
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Description

Ceribell Delirium Monitor System by Ceribell, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251936
Clearance Date2025-12-08
Clearance TypeTraditional
Product CodeNCG
Regulation Number882.1440

Categories

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