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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 K926321
Device Name VARIAN C/D-SERIES CLINACS (CLINAC 600 C/D)
Applicant
Varian Assoc., Inc.
3045 Hanover St.
Palo Alto,  CA  94304 -1129
Applicant Contact CHARLES H WILL
Correspondent
Varian Assoc., Inc.
3045 Hanover St.
Palo Alto,  CA  94304 -1129
Correspondent Contact CHARLES H WILL
Regulation Number892.5050
Classification Product Code
IYE  
Date Received12/16/1992
Decision Date 08/09/1994
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
Recalls CDRH Recalls
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