FDA 510(k) Application Details - K222970

Device Classification Name	More FDA Info for this Device
510(K) Number	K222970
Device Name	LVivo IQS
Applicant	DiA Imaging Analysis Ltd 77 Haenergia Street Beer-Sheva 8470912 IL Other 510(k) Applications for this Company
Contact	Michal Yaacobi Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2022
Decision Date	02/01/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review