MYAH
K号: K222933 · 2023-06-29
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决定日期2023-06-29
产品代码MXK
咨询委员会OP
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决定实质等同
器械摘要
MYAH is the device name listed in this FDA 510(k) record. The listed applicant is Visia Imaging S.R.L.. It received FDA 510(k) clearance on 2023-06-29 under 510(k) number K222933. The device is classified under product code MXK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MYAH?
MYAH is a medical device that received FDA 510(k) clearance on 2023-06-29. The listed applicant is Visia Imaging S.R.L.. The 510(k) number is K222933.
When did MYAH receive FDA 510(k) clearance?
MYAH received FDA 510(k) clearance on 2023-06-29, under 510(k) number K222933.
Who is the listed applicant for MYAH?
The FDA 510(k) record lists Visia Imaging S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYAH?
The FDA product code for MYAH is MXK.
列明Visia Imaging S.R.L.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：MXK）
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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