K-number	K031326
Device name	IMAGINE REFLEX
Applicant	Wieland Dental + Technik GmbH & Co. KG
Product code	EIH
Device class	Class II
Decision date	Jun 17, 2003
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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IMAGINE REFLEX

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