Class Class II

DeepRESP (K252330)

K252330 2025-11-17 Traditional
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Description

DeepRESP by Nox Medical Ehf, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252330
Clearance Date2025-11-17
Clearance TypeTraditional
Product CodeOLZ
Regulation Number882.1400

Categories

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