FDA 510(k)

ARTIS icono 地板; ARTIS icono 双平面; ARTIS icono 天花板; ARTIS pheno

K号: K254173 · 2026-04-24

决定日期2026-04-24

产品代码OWB

咨询委员会RA

决定实质等同

器械摘要

ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2026-04-24 under 510(k) number K254173. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno?

ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno is a medical device that received FDA 510(k) clearance on 2026-04-24. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K254173.

When did ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno receive FDA 510(k) clearance?

ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno received FDA 510(k) clearance on 2026-04-24, under 510(k) number K254173.

Who is the listed applicant for ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno?

FDA 510(k)记录中列出西门子医疗解决方案美国公司（Siemens Medical Solutions USA, Inc.）为申请人。这本身并不能确立该设备的制造商。

What is the FDA product code for ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno?

The FDA product code for ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS pheno is OWB.

列明Siemens Medical Solutions USA, Inc.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。

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