FDA 510(k) Applications Submitted by Susan Quick

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130278	02/05/2013	MR PERMEABILITY	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K160743	03/17/2016	Philips Ingenuity CT	Philips Medical Systems (Cleveland), Inc.
K140666	03/18/2014	MR ELASTOGRAPHY	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K131241	05/01/2013	SWIP	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K132524	08/12/2013	CT TRANSCATHETER AORTIC VALVE IMPLANTATION (TAVI) PLANNING APPLICATION	PHILIPS MEDICAL SYSTEMS
K223442	11/14/2022	MR 5300 and MR 7700 R11 MR Systems	Philips Medical Systems Nederlands B.V.
K133526	11/15/2013	MDIXON-QUANT	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K133603	11/25/2013	PHILIPS CT DYNAMIC MYOCARDIAL PERFUSION (DMP) APPLICATION	PHILIPS MEDICAL SYSTEMS