Bright Temporary C&B
K号: K192830 · 2020-09-02
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器械摘要
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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