FDA 510(k) Applications Submitted by LISELOTTE KORNMANN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130893	04/01/2013	XPERCT REL. 3	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K251397	05/06/2025	Ingenia, Ingenia CX, Ingenia Elition, Ingenia Ambition, BlueSeal, MR 5300 and MR 7700 MR System	Philips Medical Systems Nederland B.V.
K151598	06/12/2015	VesselNavigator Rel. 1.0	PHILIPS MEDICAL SYSTEMS NEDERLAND BV
K132147	07/11/2013	2D PERFUSION	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K212175	07/12/2021	DynaCAD	Invivo Corporation
K132305	07/24/2013	STENTBOOST REL. 4	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K142126	08/04/2014	EP NAVIGATOR REL. 5.0	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K142273	08/15/2014	EmboGuide	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K192259	08/21/2019	Philips IntelliSite Pathology Solution	Philips Electronics Nederland B.V.
K232762	09/08/2023	dS Breast Coil 7ch 1.5T	Invivo Corporation (Business Trade Name: Philips)
K233204	09/28/2023	Philips IntelliSite Pathology Solution 5.1	Philips Medical Systems Nederland B.V.
K203845	12/31/2020	Philips IntelliSite Pathology Solution	Philips Medical Systems Nederland B.V.