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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 K232381
Device Name LOGIQ Totus
Applicant
GE Medical Systems Ultrasound and Primary care Diagnostics,
LLC
9900 Innovation Drive
Wauwatosa,  WI  53226
Applicant Contact Bryan Behn
Correspondent
GE Medical Systems Ultrasound and Primary care Diagnostics,
LLC
9900 Innovation Drive
Wauwatosa,  WI  53226
Correspondent Contact Bryan Behn
Regulation Number892.1550
Classification Product Code
IYN  
Subsequent Product Codes
ITX   IYO   QIH  
Date Received08/08/2023
Decision Date 12/07/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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