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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 K190841
Device Name SCENARIA View
Applicant
Hitachi Healthcare Americas
1959 Summit Commerce Park
Twinsburg,  OH  44087
Applicant Contact Aaron Pierce
Correspondent
Hitachi Healthcare Americas
1959 Summit Commerce Park
Twinsburg,  OH  44087
Correspondent Contact Aaron Pierce
Regulation Number892.1750
Classification Product Code
JAK  
Date Received04/01/2019
Decision Date 09/13/2019
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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