K-number	K232030
Device name	Ingenia Elition R5.7.1 SP4 MR Systems
Applicant	Philips Medical Systems Nederland B.V.
Product code	LNH
Device class	Class II
Decision date	Aug 2, 2023
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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Ingenia Elition R5.7.1 SP4 MR Systems

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