K-number	K230933
Device name	REMI Remote EEG Monitoring System
Applicant	Epitel, Inc.
Product code	OMC
Device class	Class II
Decision date	Jun 30, 2023
Decision	Substantially Equivalent
Regulation	882.1400

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Source

View the full FDA submission: accessdata.fda.gov

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REMI Remote EEG Monitoring System

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