FDA 510(k) Application Details - K231366

Device Classification Name	Electroencephalograph   More FDA Info for this Device
510(K) Number	K231366
Device Name	Electroencephalograph
Applicant	BioSerenity SAS 47, avenue de l'H⌠pital ICM-iPEPS Paris 75013 FR Other 510(k) Applications for this Company
Contact	Madubuike Okafor Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	GWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/11/2023
Decision Date	11/09/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review