FDA 510(k) Application Details - DEN210014

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN210014
Device Name	EaseVRx
Applicant	AppliedVR, Inc. 16760 Stagg St, Ste 216 Van Nuys, CA 91406 US Other 510(k) Applications for this Company
Contact	Jafar Shenasa Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QRA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/30/2021
Decision Date	11/16/2021
Decision	DENG -
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status
Type	Direct
Reviewed By Third Party	N
Expedited Review