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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Microscope, Automated, Image Analysis, Immunohistochemistry,Operator Intervention,Nuclear Intensity & Percent Positivity
510(k) Number K122143
Device Name VIRTUOSO SYSTEM FOR IHC PR (1E2) BENCHMARK ULTRA STAINER
Applicant
Ventana Medical Systems, Inc.
575 Shirlynn Court
Los Angeles,  CA  94022
Applicant Contact Erika B Ammirati
Correspondent
Ventana Medical Systems, Inc.
575 Shirlynn Court
Los Angeles,  CA  94022
Correspondent Contact Erika B Ammirati
Regulation Number864.1860
Classification Product Code
NQN  
Subsequent Product Codes
NOT   OEO  
Date Received07/19/2012
Decision Date 09/19/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Pathology
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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