FDA 510(k) Applications Submitted by Kevin Kong

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170315	02/01/2017	Acuson SC2000 Diagnostic Ultrasound System	Siemens Medical Solutions Inc.
K171766	06/14/2017	Acuson SC2000 Diagnostic Ultrasound System	Siemens Medical Solutions Inc.
K142628	09/16/2014	Acuson SC2000 Diagnostic Ultrasound System	SIEMENS MEDICAL SOLUTIONS, INC.
K123039	09/28/2012	CDI BLOOD PARAMETER MONITORING SYSTEM 500	TERUMO CARDIOVASCULAR SYSTEMS CORP.
K203358	11/16/2020	Solitaire X Revascularization Device	Micro Therapeutics, Inc d/b/a ev3 Neurovascular
K133658	11/27/2013	CDI BLOOD PARAMETER MONITORING SYSTEM 500	TERUMO CARDIOVASCULAR SYSTEMS CORP.