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FDA 510(k)

SOMATOM X.cite; SOMATOM X.ceed

K 號：K253574 · 2026-03-20

申請人Siemens Medical Solutions USA, Inc.
決定日期2026-03-20
產品代碼JAK
諮詢委員會RA
決定Substantially Equivalent

器材摘要

SOMATOM X.cite; SOMATOM X.ceed 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 2026-03-20 under 510(k) number K253574. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SOMATOM X.cite; SOMATOM X.ceed?

SOMATOM X.cite; SOMATOM X.ceed is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K253574.

When did SOMATOM X.cite; SOMATOM X.ceed receive FDA 510(k) clearance?

SOMATOM X.cite; SOMATOM X.ceed received FDA 510(k) clearance on 2026-03-20, under 510(k) number K253574.

Who is the listed applicant for SOMATOM X.cite; SOMATOM X.ceed?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOMATOM X.cite; SOMATOM X.ceed?

The FDA product code for SOMATOM X.cite; SOMATOM X.ceed is JAK.

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相關器械（代碼：JAK）

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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