FDA 510(k)

visio.lign 颜色，visio.lign 防护罩

K号: K240735 · 2024-12-12

决定日期2024-12-12

产品代码EBD

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决定实质等同

器械摘要

visio.lign color, visio.lign shield is the device name listed in this FDA 510(k) record. The listed applicant is Bredent GmbH & Co. KG. It received FDA 510(k) clearance on 2024-12-12 under 510(k) number K240735. 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 visio.lign color, visio.lign shield?

visio.lign color, visio.lign shield is a medical device that received FDA 510(k) clearance on 2024-12-12. The listed applicant is Bredent GmbH & Co. KG. The 510(k) number is K240735.

When did visio.lign color, visio.lign shield receive FDA 510(k) clearance?

visio.lign color, visio.lign shield received FDA 510(k) clearance on 2024-12-12, under 510(k) number K240735.

Who is the listed applicant for visio.lign color, visio.lign shield?

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

What is the FDA product code for visio.lign color, visio.lign shield?

The FDA product code for visio.lign color, visio.lign shield is EBD.

列明Bredent GmbH & Co. KG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。

K152113BioHPP - breCAM.BioHPP

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