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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, nuclear magnetic resonance imaging
510(k) Number K192924
Device Name MAGNETOM Vida, MAGNETOM Lumina, MAGNETOM Vida Fit
Applicant
Siemens Medical Solutions USA Inc.
40 Liberty Boulevard, MailCode 65-1A
Malvern,  PA  19355
Applicant Contact Andrew Turner
Correspondent
Siemens Medical Solutions USA Inc.
40 Liberty Boulevard, MailCode 65-1A
Malvern,  PA  19355
Correspondent Contact Andrew Turner
Regulation Number892.1000
Classification Product Code
LNH  
Subsequent Product Codes
LNI   MOS  
Date Received10/16/2019
Decision Date 03/11/2020
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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