FDA 510(k) Application Details - K183692

Device Classification Name	Interferential Current Therapy   More FDA Info for this Device
510(K) Number	K183692
Device Name	Interferential Current Therapy
Applicant	Vision Quest Industries Inc./ dba VQ OrthoCare 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	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/31/2018
Decision Date	06/12/2019
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