Class Class II

Myocene (DEN230051)

DEN230051 2025-01-17 Direct
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Description

Myocene by Myocene, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberDEN230051
Clearance Date2025-01-17
Clearance TypeDirect
Product CodeSDX
Regulation Number882.1871

Categories

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