K-number	K070723
Device name	FUTURABOND DC/SINGLE DOSE
Applicant	Voco GmbH
Product code	KLE
Device class	Class II
Decision date	Jun 7, 2007
Decision	Substantially Equivalent
Regulation	872.3200

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View the full FDA submission: accessdata.fda.gov

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FUTURABOND DC/SINGLE DOSE

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