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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.
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