Class Class II

Paradigm System (K252950)

K252950 2025-12-15 Traditional
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Description

Paradigm System by Proprio, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252950
Clearance Date2025-12-15
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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