K-number	K153022
Device name	Philips IntelliSpace Cardiovascular
Applicant	Philips Medical Systems Nethrlands BV
Product code	LLZ
Device class	Class II
Decision date	Nov 18, 2015
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Philips IntelliSpace Cardiovascular

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