肿瘤视野Viz
K号: K251766 · 2025-07-08
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器械摘要
TumorSight Viz is the device name listed in this FDA 510(k) record. The listed applicant is SimBioSys, Inc.. It received FDA 510(k) clearance on 2025-07-08 under 510(k) number K251766. 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 TumorSight Viz?
TumorSight Viz is a medical device that received FDA 510(k) clearance on 2025-07-08. The listed applicant is SimBioSys, Inc.. The 510(k) number is K251766.
When did TumorSight Viz receive FDA 510(k) clearance?
TumorSight Viz received FDA 510(k) clearance on 2025-07-08, under 510(k) number K251766.
Who is the listed applicant for TumorSight Viz?
FDA 510(k)记录中列出SimBioSys，Inc.为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for TumorSight Viz?
The FDA product code for TumorSight Viz is QIH.
相关临床试验
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。
列明SimBioSys, 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：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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