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FDA 510(k)

DeepFoqus (DeepFoqus-Accelerate)

K号: K241982 · 2025-04-04

申请人Foqus Technologies, Inc.
决定日期2025-04-04
产品代码QIH
咨询委员会RA
决定实质等同

器械摘要

DeepFoqus (DeepFoqus-Accelerate) is the device name listed in this FDA 510(k) record. The listed applicant is Foqus Technologies, Inc.. It received FDA 510(k) clearance on 2025-04-04 under 510(k) number K241982. 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 DeepFoqus (DeepFoqus-Accelerate)?

DeepFoqus (DeepFoqus-Accelerate) is a medical device that received FDA 510(k) clearance on 2025-04-04. The listed applicant is Foqus Technologies, Inc.. The 510(k) number is K241982.

When did DeepFoqus (DeepFoqus-Accelerate) receive FDA 510(k) clearance?

DeepFoqus (DeepFoqus-Accelerate) received FDA 510(k) clearance on 2025-04-04, under 510(k) number K241982.

Who is the listed applicant for DeepFoqus (DeepFoqus-Accelerate)?

The FDA 510(k) record lists Foqus Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DeepFoqus (DeepFoqus-Accelerate)?

The FDA product code for DeepFoqus (DeepFoqus-Accelerate) is QIH.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

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。

K260055syngo.CT 脑部量化Siemens Medical Solutions USA, Inc.K262390骨专家VisianaK261368快速平台（R6.7）Ischemaview, Inc.K261623EchoPAC软件仅用 / EchoPAC插件（v211）GE Medical Systems Ultrasound and Primary Care DiagnosticsK261677人工智能肾脏评估（AIRA）版本 1Aramis Global AI Consultancies, LLCK2608794DMINVIA, LLC

官方来源

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