FDA 510(k) Application Details - K201824

Device Classification Name	More FDA Info for this Device
510(K) Number	K201824
Device Name	Nerivio
Applicant	Theranica Bio-Electronics LTD. 4 Ha-Omanut St. Netanya 4250438 IL Other 510(k) Applications for this Company
Contact	Alon Ironi Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QGT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/01/2020
Decision Date	10/23/2020
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