K-number	K060104
Device name	PRISMATIK CLINICAL ZIRCONIA
Applicant	Glidewell Laboratories
Product code	EIH
Device class	Class II
Decision date	Mar 15, 2006
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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PRISMATIK CLINICAL ZIRCONIA

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