FDA 510(k) Applications Submitted by Maxs Newberry

FDA 510(k) Number	Submission Date	Device Name	Applicant
K162329	08/19/2016	CX50 Diagnostic Ultrasound System, Sparq Diagnostic Ultrasound System	Philips Healthcare
K172607	08/30/2017	Philips EPIQ 5 Diagnostic Ultrasound System, EPIQ 7 Diagnostic Ultrasound System, Affiniti 30 Diagnostic Ultrasound System, Affiniti 50 Diagnostic Ultrasound System, Affiniti 70 Diagnostic Ultrasound System	Philips Healthcare