彩虹MCT
K号: K200270 · 2021-04-16
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器械摘要
rainbow MCT is the device name listed in this FDA 510(k) record. The listed applicant is Dentium Co., Ltd (Ict Branch). It received FDA 510(k) clearance on 2021-04-16 under 510(k) number K200270. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the rainbow MCT?
rainbow MCT is a medical device that received FDA 510(k) clearance on 2021-04-16. The listed applicant is Dentium Co., Ltd (Ict Branch). The 510(k) number is K200270.
When did rainbow MCT receive FDA 510(k) clearance?
rainbow MCT received FDA 510(k) clearance on 2021-04-16, under 510(k) number K200270.
Who is the listed applicant for rainbow MCT?
The FDA 510(k) record lists Dentium Co., Ltd (Ict Branch) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for rainbow MCT?
The FDA product code for rainbow MCT is OAS.
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Dentium Co., Ltd (Ict Branch)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：OAS）
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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