Class Class II

BE Plus PRO, Neurotravel LIGHT (K242305)

K242305 2024-09-04 Special
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Description

BE Plus PRO, Neurotravel LIGHT by Eb Neuro S.P.A. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242305
Clearance Date2024-09-04
Clearance TypeSpecial
Product CodeGWL
Regulation Number882.1835

Categories

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