Class Class II

Intellidrop (K251598)

K251598 2025-12-10 Traditional
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Description

Intellidrop by Brainspace, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251598
Clearance Date2025-12-10
Clearance TypeTraditional
Product CodeJXG
Regulation Number882.5550

Categories

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