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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 K171128
Device Name SIGNA Premier
Applicant
GE Medical Systems, LLC
3200 Grandview Blvd
Waukesha,  WI  53188
Applicant Contact Mary A. Mayka
Correspondent
GE Medical Systems, LLC
3200 Grandview Blvd
Waukesha,  WI  53188
Correspondent Contact Mary A. Mayka
Regulation Number892.1000
Classification Product Code
LNH  
Subsequent Product Codes
LNI   MOS  
Date Received04/17/2017
Decision Date 07/14/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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