Viz AAA
K号: K223443 · 2023-03-17
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器械摘要
Viz AAA is the device name listed in this FDA 510(k) record. The listed applicant is Viz. Ai, Inc.. It received FDA 510(k) clearance on 2023-03-17 under 510(k) number K223443. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Viz AAA?
Viz AAA is a medical device that received FDA 510(k) clearance on 2023-03-17. The listed applicant is Viz. Ai, Inc.. The 510(k) number is K223443.
When did Viz AAA receive FDA 510(k) clearance?
Viz AAA received FDA 510(k) clearance on 2023-03-17, under 510(k) number K223443.
Who is the listed applicant for Viz AAA?
The FDA 510(k) record lists Viz. Ai, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Viz AAA?
The FDA product code for Viz AAA is QFM.
列明Viz. Ai, Inc.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：QFM）
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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