K-number	K060756
Device name	MEDLOG, MODEL 1-0-10
Applicant	Bmc Gesellschaft Fur Medizintechnik Mbh
Product code	MWI
Device class	Class II
Decision date	Oct 30, 2006
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MEDLOG, MODEL 1-0-10

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