Class Class II

Pixie Pulse (SM9068) (K241365)

K241365 2024-08-12 Traditional
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Description

Pixie Pulse (SM9068) by Pixie Cup, LLC — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241365
Clearance Date2024-08-12
Clearance TypeTraditional
Product CodeNUH
Regulation Number882.5890

Categories

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