Evogue 牙科单元
K号: K152100 · 2016-01-22
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决定日期2016-01-22
产品代码EIA
咨询委员会DE
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器械摘要
Evogue Dental Unit is the device name listed in this FDA 510(k) record. The listed applicant is Takara Belmont Corporation. It received FDA 510(k) clearance on 2016-01-22 under 510(k) number K152100. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Evogue Dental Unit?
Evogue Dental Unit is a medical device that received FDA 510(k) clearance on 2016-01-22. The listed applicant is Takara Belmont Corporation. The 510(k) number is K152100.
When did Evogue Dental Unit receive FDA 510(k) clearance?
Evogue Dental Unit received FDA 510(k) clearance on 2016-01-22, under 510(k) number K152100.
Who is the listed applicant for Evogue Dental Unit?
The FDA 510(k) record lists Takara Belmont Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Evogue Dental Unit?
The FDA product code for Evogue Dental Unit is EIA.
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Takara Belmont Corporation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：EIA）
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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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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