TumorSight Viz
K号: K243189 · 2024-10-25
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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 2024-10-25 under 510(k) number K243189. 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 2024-10-25. The listed applicant is SimBioSys, Inc.. The 510(k) number is K243189.
When did TumorSight Viz receive FDA 510(k) clearance?
TumorSight Viz received FDA 510(k) clearance on 2024-10-25, under 510(k) number K243189.
Who is the listed applicant for TumorSight Viz?
The FDA 510(k) record lists SimBioSys, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TumorSight Viz?
The FDA product code for TumorSight Viz is QIH.
相关临床试验
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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。
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官方来源
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