K-number	K013470
Device name	MODIFICATION TO M2376A DEVICELINK SYSTEM
Applicant	Philips Medical Systems, Inc.
Product code	MWI
Device class	Class II
Decision date	Nov 14, 2001
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO M2376A DEVICELINK SYSTEM

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