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FDA 510(k)

Bright Temporary C&B

K号: K192830 · 2020-09-02

决定日期2020-09-02
产品代码EBG
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决定实质等同

器械摘要

Bright Temporary C&B is the device name listed in this FDA 510(k) record. The listed applicant is Dmp Dental Industry S.A.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K192830. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Bright Temporary C&B?

Bright Temporary C&B is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is Dmp Dental Industry S.A.. The 510(k) number is K192830.

When did Bright Temporary C&B receive FDA 510(k) clearance?

Bright Temporary C&B received FDA 510(k) clearance on 2020-09-02, under 510(k) number K192830.

Who is the listed applicant for Bright Temporary C&B?

The FDA 510(k) record lists Dmp Dental Industry S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bright Temporary C&B?

The FDA product code for Bright Temporary C&B is EBG.

相关临床试验

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。

列明Dmp Dental Industry S.A.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。

相关器械(代码:EBG)

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。

官方来源

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