Class Class II

actiTENS mini (K252767)

K252767 2026-01-16 Traditional
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Description

actiTENS mini by Sublimed, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252767
Clearance Date2026-01-16
Clearance TypeTraditional
Product CodeGZJ
Regulation Number882.5890

Categories

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