K-number	K242305
Device name	BE Plus PRO, Neurotravel LIGHT
Applicant	Eb Neuro S.P.A.
Product code	GWL
Device class	Class II
Decision date	Sep 4, 2024
Decision	Substantially Equivalent
Regulation	882.1835

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Source

View the full FDA submission: accessdata.fda.gov

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BE Plus PRO, Neurotravel LIGHT

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