Seg Pro V3 (RT-300)
K号: K251306 · 2026-01-28
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器械摘要
Seg Pro V3 (RT-300) is the device name listed in this FDA 510(k) record. The listed applicant is Ever Fortune.Ai, Co., Ltd.. It received FDA 510(k) clearance on 2026-01-28 under 510(k) number K251306. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Seg Pro V3 (RT-300)?
Seg Pro V3 (RT-300) is a medical device that received FDA 510(k) clearance on 2026-01-28. The listed applicant is Ever Fortune.Ai, Co., Ltd.. The 510(k) number is K251306.
When did Seg Pro V3 (RT-300) receive FDA 510(k) clearance?
Seg Pro V3 (RT-300) received FDA 510(k) clearance on 2026-01-28, under 510(k) number K251306.
Who is the listed applicant for Seg Pro V3 (RT-300)?
The FDA 510(k) record lists Ever Fortune.Ai, Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Seg Pro V3 (RT-300)?
The FDA product code for Seg Pro V3 (RT-300) is QKB.
列明Ever Fortune.Ai, Co., Ltd.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：QKB）
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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