K-number	K130184
Device name	ZENOLUX
Applicant	Wieland Dental + Technik GmbH & Co. KG
Product code	EIH
Device class	Class II
Decision date	May 24, 2013
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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ZENOLUX

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