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FDA 510(k) Applications Submitted by PHILIPS MEDICAL SYSTEMS, NEDERLAND B.V.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230972
04/05/2023
Ingenia Elition and MR 7700 MR Systems
Philips Medical Systems, Nederland B.V.
K143253
11/13/2014
O-MAR
PHILIPS MEDICAL SYSTEMS, NEDERLAND B.V.
K201583
06/11/2020
SmartCT R1.0
Philips Medical Systems, Nederland B.V.
K193454
12/13/2019
IQon Spectral CT
Philips Medical Systems, Nederland B.V.
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