K-number	K073140
Device name	VITALOGIK MODEL 4000/4500
Applicant	Mennen Medical , Ltd.
Product code	DSI
Device class	Class II
Decision date	Nov 21, 2007
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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VITALOGIK MODEL 4000/4500

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