FDA 510(k) Applications Submitted by Michael Chambers

FDA 510(k) Number	Submission Date	Device Name	Applicant
K240850	03/27/2024	EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems	Philips Ultrasound LLC
K240980	04/10/2024	EPIQ Series Diagnostic Ultrasound System	Philips Ultrasound LLC
K233545	11/03/2023	EPIQ Series Diagnostic Ultrasound System	Philips Ultrasound LLC
K233788	11/28/2023	EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System	Philips Ultrasound LLC