血管辅助闭塞分级（VAOT）（v1.0）
K号: K260729 · 2026-06-18
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器械摘要
Vascular Assist Occlusion Triage (VAOT) (v1.0) is the device name listed in this FDA 510(k) record. The listed applicant is GuideAI Health. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K260729. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Vascular Assist Occlusion Triage (VAOT) (v1.0)?
Vascular Assist Occlusion Triage (VAOT) (v1.0) is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is GuideAI Health. The 510(k) number is K260729.
When did Vascular Assist Occlusion Triage (VAOT) (v1.0) receive FDA 510(k) clearance?
Vascular Assist Occlusion Triage (VAOT) (v1.0) received FDA 510(k) clearance on 2026-06-18, under 510(k) number K260729.
Who is the listed applicant for Vascular Assist Occlusion Triage (VAOT) (v1.0)?
The FDA 510(k) record lists GuideAI Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vascular Assist Occlusion Triage (VAOT) (v1.0)?
The FDA product code for Vascular Assist Occlusion Triage (VAOT) (v1.0) is QAS.
相关临床试验
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相关器械（代码：QAS）
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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