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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Planning, Radiation Therapy Treatment
510(k) Number K123152
Device Name VITESSE 3.0
Applicant
Varian Medical Systems, Oncology Systems
911 Hansen Way
Palo Alto,  CA  94304
Applicant Contact VY TRAN
Correspondent
Varian Medical Systems, Oncology Systems
911 Hansen Way
Palo Alto,  CA  94304
Correspondent Contact VY TRAN
Regulation Number892.5050
Classification Product Code
MUJ  
Date Received10/09/2012
Decision Date 12/07/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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