FDA 510(k)

CINA

K号: K221716 · 2022-11-22

决定日期2022-11-22

产品代码QAS

咨询委员会RA

决定实质等同

器械摘要

CINA is the device name listed in this FDA 510(k) record. The listed applicant is Avicenna.Ai. It received FDA 510(k) clearance on 2022-11-22 under 510(k) number K221716. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CINA?

CINA is a medical device that received FDA 510(k) clearance on 2022-11-22. The listed applicant is Avicenna.Ai. The 510(k) number is K221716.

When did CINA receive FDA 510(k) clearance?

CINA received FDA 510(k) clearance on 2022-11-22, under 510(k) number K221716.

Who is the listed applicant for CINA?

The FDA 510(k) record lists Avicenna.Ai as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CINA?

The FDA product code for CINA is QAS.

列明Avicenna.Ai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。

K240942CINA-CSpine K240612CINA-VCF K233342CINA-ASPECTS K233968CINA-iPE K210237CINA 胸部 K200855CINA

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官方来源

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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。