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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, X-Ray, Tomography, Computed
510(k) Number K221727
Device Name syngo.CT Extended Functionality
Applicant
Siemens Medical Solutions USA, Inc.
810 innovation Drive
Knoxville,  TN  37932
Applicant Contact Monsuru Bello
Correspondent
Siemens Medical Solutions USA, Inc.
810 innovation Drive
Knoxville,  TN  37932
Correspondent Contact Monsuru Bello
Regulation Number892.1750
Classification Product Code
JAK  
Date Received06/14/2022
Decision Date 07/13/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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