K-number	K193436
Device name	VITA Ambria
Applicant	Vita Zahnfabrik GmbH H Rauter & CO
Product code	EIH
Device class	Class II
Decision date	May 14, 2020
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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VITA Ambria

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