K-number	K000710
Device name	MD 10, SEM, SM 12, CBM
Applicant	NOUVAG AG
Product code	EFB
Device class	Class I
Decision date	May 11, 2000
Decision	Substantially Equivalent
Regulation	872.4200

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View the full FDA submission: accessdata.fda.gov

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MD 10, SEM, SM 12, CBM

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