Class Class II

Aura Glide (FC40) (K252187)

K252187 2025-12-23 Traditional
Home/ Devices/ Aura Glide (FC40) (K252187)

Description

Aura Glide (FC40) by Aura Medical, LLC, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252187
Clearance Date2025-12-23
Clearance TypeTraditional
Product CodeNFO
Regulation Number882.5890

Categories

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