FDA 510(k) Application Details - K162392

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K162392
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	AVAZZIA, INC. 13140 COIT ROAD SUITE 515 DALLAS, TX 75240 US Other 510(k) Applications for this Company
Contact	TAMMY LAHUTSKY Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/26/2016
Decision Date	05/12/2017
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