K-number	K113125
Device name	INTELLIVUE MX40 PATIENT MONITOR
Applicant	Philips Medical Systems
Product code	DSI
Device class	Class II
Decision date	Nov 17, 2011
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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INTELLIVUE MX40 PATIENT MONITOR

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