FDA 510(k)

VITA Akzent LC

K号: K211854 · 2021-11-22

决定日期2021-11-22

产品代码EBD

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决定实质等同

器械摘要

VITA Akzent LC is the device name listed in this FDA 510(k) record. The listed applicant is Vita Zahnfabrik GmbH H Rauter & CO. It received FDA 510(k) clearance on 2021-11-22 under 510(k) number K211854. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the VITA Akzent LC?

VITA Akzent LC is a medical device that received FDA 510(k) clearance on 2021-11-22. The listed applicant is Vita Zahnfabrik GmbH H Rauter & CO. The 510(k) number is K211854.

When did VITA Akzent LC receive FDA 510(k) clearance?

VITA Akzent LC received FDA 510(k) clearance on 2021-11-22, under 510(k) number K211854.

Who is the listed applicant for VITA Akzent LC?

The FDA 510(k) record lists Vita Zahnfabrik GmbH H Rauter & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITA Akzent LC?

The FDA product code for VITA Akzent LC is EBD.

列明Vita Zahnfabrik GmbH H Rauter & CO为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K193434VITA LUMEX AC K193436VITA Ambria

官方来源

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