CINA-iPE
K号: K233968 · 2024-03-13
广告
器械摘要
CINA-iPE is the device name listed in this FDA 510(k) record. The listed applicant is Avicenna.Ai. It received FDA 510(k) clearance on 2024-03-13 under 510(k) number K233968. 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-iPE?
CINA-iPE is a medical device that received FDA 510(k) clearance on 2024-03-13. The listed applicant is Avicenna.Ai. The 510(k) number is K233968.
When did CINA-iPE receive FDA 510(k) clearance?
CINA-iPE received FDA 510(k) clearance on 2024-03-13, under 510(k) number K233968.
Who is the listed applicant for CINA-iPE?
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-iPE?
The FDA product code for CINA-iPE 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。
相关器械（代码：QAS）
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。
广告