K-number	K071410
Device name	ARGEN PEARL BRAND ZIRCONIA
Applicant	The Argen Corporation
Product code	EIH
Device class	Class II
Decision date	Aug 15, 2007
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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ARGEN PEARL BRAND ZIRCONIA

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