FDA 510(k) Application Details - K123540

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K123540
Device Name	System, X-Ray, Tomography, Computed
Applicant	SIEMENS MEDICAL SYSTEMS, INC. 51 VALLEY STREAM PARKWAY MALVERN, PA 19355-1406 US Other 510(k) Applications for this Company
Contact	KIMBERLY MANGUM Other 510(k) Applications for this Contact
Regulation Number	892.1750   More FDA Info for this Regulation Number
Classification Product Code	JAK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/19/2012
Decision Date	08/29/2013
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