FDA 510(k) Application Details - K240769

Device Classification Name	More FDA Info for this Device
510(K) Number	K240769
Device Name	LVivo IQS
Applicant	DiA Imaging Analysis Ltd. HaEnergia Street 77 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	03/21/2024
Decision Date	05/24/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review