K-number	K093744
Device name	EXCITE F AND EXCITE DSC
Applicant	Ivoclar Vivadent, Inc.
Product code	KLE
Device class	Class II
Decision date	Mar 10, 2010
Decision	Substantially Equivalent
Regulation	872.3200

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Source

View the full FDA submission: accessdata.fda.gov

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EXCITE F AND EXCITE DSC

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