CT:VQ
K号: K251484 · 2025-08-28
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器械摘要
CT:VQ is the device name listed in this FDA 510(k) record. The listed applicant is 4Dmedical Limited. It received FDA 510(k) clearance on 2025-08-28 under 510(k) number K251484. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CT:VQ?
CT:VQ is a medical device that received FDA 510(k) clearance on 2025-08-28. The listed applicant is 4Dmedical Limited. The 510(k) number is K251484.
When did CT:VQ receive FDA 510(k) clearance?
CT:VQ received FDA 510(k) clearance on 2025-08-28, under 510(k) number K251484.
Who is the listed applicant for CT:VQ?
The FDA 510(k) record lists 4Dmedical Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CT:VQ?
The FDA product code for CT:VQ is JAK.
列明4Dmedical Limited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：JAK）
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。
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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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