510(k) K223458

Device
Ingenia, Ingenia CX, Ingenia Elition, Ingenia Ambition, MR 5300 and MR 7700 MR Systems
Applicant
Philips Medical Systems Nederland B.V.
510(k) number
K223458
Product code
LNH
Decision
Substantially Equivalent (SESE)
Decision date
2023-04-06
Date received
2022-11-16
Regulation
892.1000
Classification name
System, Nuclear Magnetic Resonance Imaging
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Ioana Ulea
Address
Veenpluis 6 Best NL 5684PC 5684PC

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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