Class Class II

Canvas Dx (K243558)

K243558 2025-04-11 Traditional
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Description

Canvas Dx by Cognoa, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243558
Clearance Date2025-04-11
Clearance TypeTraditional
Product CodeQPF
Regulation Number882.1491

Categories

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