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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name system, imaging, pulsed doppler, ultrasonic
510(k) Number K223387
Device Name V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System
Samsung Medison Co., Ltd.
3366, Hanseo-ro, Nam-myeon
Hongcheon-gun,  KR 25108
Applicant Contact Ju Jee Young
Samsung Medison Co. Ltd.
3366, Hanseo-ro, Nam-myeon
Hongcheon-gun,  KR 25108
Correspondent Contact Ju Jee Young
Regulation Number892.1550
Classification Product Code
Subsequent Product Codes
Date Received11/07/2022
Decision Date 02/13/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No