FDA 510(k) Application Details - K233166

Device Classification Name	More FDA Info for this Device
510(K) Number	K233166
Device Name	NET Recovery Corp/NET Device
Applicant	Net Recovery 155 N Riverview Dr, Suite 114 Anaheim Hills, CA 92808 US Other 510(k) Applications for this Company
Contact	Joe Winston Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PZR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2023
Decision Date	05/29/2024
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