FDA 510(k) Application Details - K142236

Device Classification Name	Stimulator, Electrical, Transcutaneous, For Arthritis   More FDA Info for this Device
510(K) Number	K142236
Device Name	Stimulator, Electrical, Transcutaneous, For Arthritis
Applicant	VISION QUEST INDUSTRIES, INC. 1390 DECISION STREET, SUITE A VISTA, CA 92081 US Other 510(k) Applications for this Company
Contact	MOHAMED OUERGHI Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NYN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/13/2014
Decision Date	03/23/2015
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