FDA 510(k) Application Details - K230950

Device Classification Name	More FDA Info for this Device
510(K) Number	K230950
Device Name	ARTIS icono (VE30A)
Applicant	Siemens Medical Solutions USA, Inc. 40 Liberty Boulevard Malvern, PA 19355 US Other 510(k) Applications for this Company
Contact	Patricia D. Jones Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/04/2023
Decision Date	12/14/2023
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