Class Class II

Daylight (K233872)

K233872 2024-08-30 Traditional
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Description

Daylight by Big Health, Inc. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233872
Clearance Date2024-08-30
Clearance TypeTraditional
Product CodeSCP
Regulation Number882.5801

Categories

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