K-number	K223442
Device name	MR 5300 and MR 7700 R11 MR Systems
Applicant	Philips Medical Systems Nederlands B.V.
Product code	LNH
Device class	Class II
Decision date	Dec 23, 2022
Decision	Substantially Equivalent
Regulation	892.1000

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Source

View the full FDA submission: accessdata.fda.gov

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MR 5300 and MR 7700 R11 MR Systems

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