Nanox.ARC X
K号: K250850 · 2025-04-16
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器械摘要
Nanox.ARC X is the device name listed in this FDA 510(k) record. The listed applicant is Nano-X Imaging , Ltd.. It received FDA 510(k) clearance on 2025-04-16 under 510(k) number K250850. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nanox.ARC X?
Nanox.ARC X is a medical device that received FDA 510(k) clearance on 2025-04-16. The listed applicant is Nano-X Imaging , Ltd.. The 510(k) number is K250850.
When did Nanox.ARC X receive FDA 510(k) clearance?
Nanox.ARC X received FDA 510(k) clearance on 2025-04-16, under 510(k) number K250850.
Who is the listed applicant for Nanox.ARC X?
The FDA 510(k) record lists Nano-X Imaging , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nanox.ARC X?
The FDA product code for Nanox.ARC X is IZF.
相关临床试验
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列明Nano-X Imaging , 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：IZF）
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。
K252649TAP2DNano-X Imaging , Ltd.K252133Adaptix Ortho350Adaptix LimitedK242395Nanox.ARCNano-X Imaging , Ltd.K222934Nanox.ARCNano-X Imaging , Ltd.K221949Ortho Device, ADAPTIX 3D Orthopedic Imaging SystemPausch Medical GmbHK213081CLOT-LESS - CLOsure Tailored: LEss Antithrombotic Strategy After LAAC for Stroke PreventionGeneral Medical Merate S.P.A
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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