FDA 510(k) Application Details - K123737

Device Classification Name	System, Tomography, Computed, Emission   More FDA Info for this Device
510(K) Number	K123737
Device Name	System, Tomography, Computed, Emission
Applicant	SIEMENS MEDICAL SOLUTIONS USA, INC. 810 INNOVATION DR. KNOXVILLE, TN 37932 US Other 510(k) Applications for this Company
Contact	ALAINE MEIDO, RAC Other 510(k) Applications for this Contact
Regulation Number	892.1200   More FDA Info for this Regulation Number
Classification Product Code	KPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2012
Decision Date	01/29/2013
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