Seg Pro V3 (RT-300)
K-Number: K251306 · 2026-01-28
ApplicantEver Fortune.Ai, Co., Ltd.
Decision Date2026-01-28
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Seg Pro V3 (RT-300) is a medical device manufactured by Ever Fortune.Ai, Co., Ltd.. It received FDA 510(k) clearance on 2026-01-28 under approval number K251306. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
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. It is manufactured by Ever Fortune.Ai, Co., Ltd.. The 510(k) number is K251306.
When was Seg Pro V3 (RT-300) approved by the FDA?
Seg Pro V3 (RT-300) received FDA 510(k) clearance on 2026-01-28, under approval number K251306.
What company makes Seg Pro V3 (RT-300)?
Seg Pro V3 (RT-300) is manufactured by Ever Fortune.Ai, Co., Ltd..
What is the FDA product code for Seg Pro V3 (RT-300)?
The FDA product code for Seg Pro V3 (RT-300) is QKB.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.