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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Generator, High-Voltage, X-Ray, Diagnostic
510(k) Number K902106
Device Name VPW 2877D5, X-RAY POWER SUPPLY
Applicant
Varian Assoc., Inc.
611 Hansen Way
P.O. Box 10800
Palo Alto,  CA  94303
Applicant Contact D SIEGEL
Correspondent
Varian Assoc., Inc.
611 Hansen Way
P.O. Box 10800
Palo Alto,  CA  94303
Correspondent Contact D SIEGEL
Regulation Number892.1700
Classification Product Code
IZO  
Date Received05/08/1990
Decision Date 08/10/1990
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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