K-number	K062130
Device name	MEISINGER BENEX, MODEL BE001
Applicant	Hager& Meisinger GmbH
Product code	EMG
Device class	Class I
Decision date	Apr 16, 2007
Decision	Substantially Equivalent
Regulation	872.4565

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View the full FDA submission: accessdata.fda.gov

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MEISINGER BENEX, MODEL BE001

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