FDA 510(k) Application Details - K103606

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K103606
Device Name	Accelerator, Linear, Medical
Applicant	SIEMENS MEDICAL SOLUTIONS USA, INC. 4040 NELSON AVE. CONCORD, CA 94520 US Other 510(k) Applications for this Company
Contact	CHRISTINE DUNBAR Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	IYE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/09/2010
Decision Date	04/15/2011
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