FDA 510(k) Application Details - K212684

Device Classification Name	Normalizing Quantitative Electroencephalograph Software   More FDA Info for this Device
510(K) Number	K212684
Device Name	Normalizing Quantitative Electroencephalograph Software
Applicant	Medeia, Inc. 7 W Figueroa St, Suite 300 Santa Barbara, CA 93101 US Other 510(k) Applications for this Company
Contact	Slav Danev Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OLU Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/24/2021
Decision Date	01/28/2023
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