K-number	K231366
Device name	Neuronaute Plus
Applicant	Bioserenity Sas
Product code	GWQ
Device class	Class II
Decision date	Nov 9, 2023
Decision	Substantially Equivalent
Regulation	882.1400

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Source

View the full FDA submission: accessdata.fda.gov

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Neuronaute Plus

Everything you need for a 510(k) submission. Nothing you don't.