FDA 510(k) Application Details - K243417

Device Classification Name	More FDA Info for this Device
510(K) Number	K243417
Device Name	RelieVRx
Applicant	AppliedVR 16760 Stagg St Van Nuys, CA 91406 US Other 510(k) Applications for this Company
Contact	Michael Chibbaro 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	11/04/2024
Decision Date	12/04/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review