FDA 510(k) Application Details - K140530

Device Classification Name	Stimulator, Electro-Acupuncture   More FDA Info for this Device
510(K) Number	K140530
Device Name	Stimulator, Electro-Acupuncture
Applicant	NAVIGANT CONSULTING, INC. 30 S WACKER DRIVE SUITE 3100 CHICAGO, IL 60606 US Other 510(k) Applications for this Company
Contact	COLLEEN HITTLE Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	BWK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/04/2014
Decision Date	10/02/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review