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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.
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)
K203845
12/31/2020
Philips IntelliSite Pathology Solution
Philips Medical Systems Nederland B.V.
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