K-number	K211854
Device name	VITA Akzent LC
Applicant	Vita Zahnfabrik GmbH H Rauter & CO
Product code	EBD
Device class	Class II
Decision date	Nov 22, 2021
Decision	Substantially Equivalent
Regulation	872.3310

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Source

View the full FDA submission: accessdata.fda.gov

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VITA Akzent LC

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