Class Class II

Nelli (Version 7.11) (K251506)

K251506 2025-11-21 Traditional
Home/ Devices/ Nelli (Version 7.11) (K251506)

Description

Nelli (Version 7.11) by Neuro Event Labs OY, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251506
Clearance Date2025-11-21
Clearance TypeTraditional
Product CodePOS
Regulation Number882.1580

Categories

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