FDA 510(k) Application Details - K231324

Device Classification Name	More FDA Info for this Device
510(K) Number	K231324
Device Name	DASI Dimensions (V1.0)
Applicant	DASI Simulations 5115 Parkcenter Ave Suite 205 Dublin, OH 43017 US Other 510(k) Applications for this Company
Contact	Sri Krishna Sivakumar 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	05/08/2023
Decision Date	01/08/2024
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