K-number	K050151
Device name	MULTIDIAGNOST ELEVA
Applicant	Philips Medical Systems North America, Inc.
Product code	KPR
Device class	Class II
Decision date	Feb 9, 2005
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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MULTIDIAGNOST ELEVA

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