虚拟锥体（1.0）
K号: K260750 · 2026-07-08
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器械摘要
Virtual Cone (1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2026-07-08 under 510(k) number K260750. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Virtual Cone (1.0)?
Virtual Cone (1.0) is a medical device that received FDA 510(k) clearance on 2026-07-08. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K260750.
When did Virtual Cone (1.0) receive FDA 510(k) clearance?
Virtual Cone (1.0) received FDA 510(k) clearance on 2026-07-08, under 510(k) number K260750.
Who is the listed applicant for Virtual Cone (1.0)?
FDA 510(k)记录中列出Varian Medical Systems, Inc.为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for Virtual Cone (1.0)?
The FDA product code for Virtual Cone (1.0) is MUJ.
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Varian Medical Systems, 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：MUJ）
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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