MAIA
K号: K153181 · 2016-06-08
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决定日期2016-06-08
产品代码MYC
咨询委员会OP
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决定实质等同
器械摘要
MAIA is the device name listed in this FDA 510(k) record. The listed applicant is Centervue S.P.A.. It received FDA 510(k) clearance on 2016-06-08 under 510(k) number K153181. The device is classified under product code MYC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MAIA?
MAIA is a medical device that received FDA 510(k) clearance on 2016-06-08. The listed applicant is Centervue S.P.A.. The 510(k) number is K153181.
When did MAIA receive FDA 510(k) clearance?
MAIA received FDA 510(k) clearance on 2016-06-08, under 510(k) number K153181.
Who is the listed applicant for MAIA?
The FDA 510(k) record lists Centervue S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAIA?
The FDA product code for MAIA is MYC.
列明Centervue S.P.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：MYC）
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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