FDA 510(k) Application Details - K081022

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K081022
Device Name	System, X-Ray, Tomography, Computed
Applicant	SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PKWY. E-50 MALVERN, PA 19355 US Other 510(k) Applications for this Company
Contact	CORRINE MCLEOD 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	04/10/2008
Decision Date	06/02/2008
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