K-number	K203216
Device name	The Multimodality Advanced Vessel Analysis
Applicant	Philips Medical Systems Nederland B.V.
Product code	JAK
Device class	Class II
Decision date	Nov 25, 2020
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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The Multimodality Advanced Vessel Analysis

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