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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 K113690
Device Name GE LOGIQ I, LOGIQ E AND VIVID E
Applicant
GE HEALTHCARE
9900 W INNOVATION DRIVE
WAUWATOSA,  WI  53226
Applicant Contact BRYAN BEHN
Correspondent
GE HEALTHCARE
9900 W INNOVATION DRIVE
WAUWATOSA,  WI  53226
Correspondent Contact BRYAN BEHN
Regulation Number892.1550
Classification Product Code
IYN  
Subsequent Product Codes
ITX   IYO  
Date Received12/15/2011
Decision Date 12/29/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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