VITA Akzent LC— 510(k) K211854

Name: FDA 510(k) clearance K211854
Creator: U.S. Food and Drug Administration
Published: 2021-11-22

Substantially Equivalent

Vita Zahnfabrik GmbH H Rauter & CO

FDA 510(k) clearance K211854 for VITA Akzent LC, Substantially Equivalent on 2021-11-22. Applicant: Vita Zahnfabrik GmbH H Rauter & CO. Device class: 2.

Clearance details

Applicant: Vita Zahnfabrik GmbH H Rauter & CO
Product code: Code EBD
Device class: Class 2
Regulation: 21 CFR 872.3310
Advisory panel: Dental
Date received: 2021-06-16
Decision date: 2021-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bad Sackingen, DE

Download summary PDF View on FDA.gov ↗

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