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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name accelerator, linear, medical
510(k) Number K962950
Device Name CADPLAN, VERSION 2.62. RADIATION THERAPY TREATMENT PLANNING SYSTEM
Applicant
VARIAN MEDICAL SYSTEMS, INC.
3045 HANOVER ST.
PALO ALTO,  CA  94304 -1120
Applicant Contact CHARLES H WILL
Correspondent
VARIAN MEDICAL SYSTEMS, INC.
3045 HANOVER ST.
PALO ALTO,  CA  94304 -1120
Correspondent Contact CHARLES H WILL
Regulation Number892.5050
Classification Product Code
IYE  
Date Received07/29/1996
Decision Date 07/22/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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