FDA 510(k)

ARTIS icono 地板; ARTIS icono 雙機; ARTIS icono 天花; ARTIS pheno

K 號：K254173 · 2026-04-24

決定日期2026-04-24

產品代碼OWB

諮詢委員會RA

決定相當於

器材摘要

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.

常見問題

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) 記錄將西门子醫療解決方案美國，股份有限公司列為申請人。這並不單獨確立設備製造商。

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.

其他以 Siemens Medical Solutions USA, Inc. 為申請人之記錄

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相關器械（代碼：OWB）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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