K-number	K122439
Device name	INTELLIVUE PATIENT MONITOR
Applicant	Philips Medizin Systeme Boeblingen GmbH
Product code	MHX
Device class	Class II
Decision date	Aug 29, 2012
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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