FDA 510(k) Applications Submitted by Philips Medical Systems Nederlands B.V.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K181966	07/23/2018	SmartPerfusion	Philips Medical Systems Nederlands B.V.
K162025	07/22/2016	IntelliSpace Portal Platform	PHILIPS MEDICAL SYSTEMS NEDERLANDS B.V.
K143128	10/30/2014	mDIXON XD	PHILIPS MEDICAL SYSTEMS NEDERLANDS B.V.
K181311	05/17/2018	Philips Hemodynamic Application R1.0	Philips Medical Systems Nederlands B.V.
K201743	06/25/2020	ClarifEye R1.0, ClarifEye Needle	Philips Medical Systems Nederlands B.V.
K223442	11/14/2022	MR 5300 and MR 7700 R11 MR Systems	Philips Medical Systems Nederlands B.V.