FDA 510(k) Application Details - K202913

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K202913
Device Name	Electrode, Cutaneous
Applicant	Memory MD Inc 125 Wilbur Place, Suite 170 Bohemia, NY 111716 US Other 510(k) Applications for this Company
Contact	Boris Goldstein Other 510(k) Applications for this Contact
Regulation Number	882.1320   More FDA Info for this Regulation Number
Classification Product Code	GXY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2020
Decision Date	03/05/2021
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