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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 K043262
Device Name GE SIGNA EXCITE MR SURGICAL OPTION
Original Applicant
GE HEALTHCARE
p.o. box 414
milwaukee,  WI  53201
Original Contact larry a kroger
Regulation Number892.1000
Classification Product Code
LNH  
Date Received11/24/2004
Decision Date 01/12/2005
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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