Class Class II

NeuroAlign software (K231897)

K231897 2025-10-21 Traditional
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Description

NeuroAlign software by Medivis, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK231897
Clearance Date2025-10-21
Clearance TypeTraditional
Product CodeHAW
Regulation Number882.4560

Categories

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