K-number	K052189
Device name	REVENEER CERAMIC REPAIR SYSTEM
Applicant	Schutz-Dental GmbH
Product code	KLE
Device class	Class II
Decision date	Oct 17, 2005
Decision	Substantially Equivalent
Regulation	872.3200

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View the full FDA submission: accessdata.fda.gov

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REVENEER CERAMIC REPAIR SYSTEM

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