K-number	K131829
Device name	INTELLIVUE PATIENT MONITOR
Applicant	Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
Product code	MHX
Device class	Class II
Decision date	Aug 16, 2013
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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INTELLIVUE PATIENT MONITOR

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