Class Class II

SomniCheck (K223676)

K223676 2023-06-01 Traditional
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Description

SomniCheck by Brainmatterz, LLC — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223676
Clearance Date2023-06-01
Clearance TypeTraditional
Product CodeGWL
Regulation Number882.1835

Categories

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