FDA 510(k)

Grandio disc 多色

K号: K261357 · 2026-04-27

决定日期2026-04-27

产品代码EBF

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决定实质等同

器械摘要

Grandio disc multicolor is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2026-04-27 under 510(k) number K261357. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Grandio disc multicolor?

Grandio disc multicolor is a medical device that received FDA 510(k) clearance on 2026-04-27. The listed applicant is Voco GmbH. The 510(k) number is K261357.

When did Grandio disc multicolor receive FDA 510(k) clearance?

Grandio disc multicolor received FDA 510(k) clearance on 2026-04-27, under 510(k) number K261357.

Who is the listed applicant for Grandio disc multicolor?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Grandio disc multicolor?

The FDA product code for Grandio disc multicolor is EBF.

列明Voco GmbH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。

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