Class Class II

SOLOPASS 2.0 System (K251317)

K251317 2025-09-05 Traditional
Home/ Devices/ SOLOPASS 2.0 System (K251317)

Description

SOLOPASS 2.0 System by Intravent Medical Partners, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251317
Clearance Date2025-09-05
Clearance TypeTraditional
Product CodeHAW
Regulation Number882.4560

Categories

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