FDA 510(k) Applications Submitted by GE MEDICAL SYSTEMS ULTRASOUND & PRIMARY CARE DIAGNOSTICS LLC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K221148	04/20/2022	Vivid iq	GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
K191112	04/26/2019	GEHC DXA Bone Densitometers with enCORE version 18	GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
K161588	06/08/2016	Vscan Extend	GE MEDICAL SYSTEMS ULTRASOUND & PRIMARY CARE DIAGNOSTICS LLC
K170714	03/09/2017	Venue	GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
K170878	03/24/2017	Vivid S60N, Vivid S70N	GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
K161224	04/29/2016	LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3	GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
K181934	07/19/2018	Vivid T8, Vivid T9	GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
K153037	10/19/2015	LOGIQ V1/ LOGIQ V2	GE MEDICAL SYSTEMS ULTRASOUND & PRIMARY CARE DIAGNOSTICS LLC