iQ解决方案
K号: K231929 · 2023-12-18
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器械摘要
iQ-solutions is the device name listed in this FDA 510(k) record. The listed applicant is Sydney Neuroimaging Analysis Centre Pty, Ltd.. It received FDA 510(k) clearance on 2023-12-18 under 510(k) number K231929. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the iQ-solutions?
iQ-solutions is a medical device that received FDA 510(k) clearance on 2023-12-18. The listed applicant is Sydney Neuroimaging Analysis Centre Pty, Ltd.. The 510(k) number is K231929.
When did iQ-solutions receive FDA 510(k) clearance?
iQ-solutions received FDA 510(k) clearance on 2023-12-18, under 510(k) number K231929.
Who is the listed applicant for iQ-solutions?
The FDA 510(k) record lists Sydney Neuroimaging Analysis Centre Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iQ-solutions?
The FDA product code for iQ-solutions is QIH.
相关临床试验
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相关器械（代码：QIH）
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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