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FDA 510(k)

syngo.CT Brain Quantification

K 號：K260055 · 2026-09-25

申請人Siemens Medical Solutions USA, Inc.
決定日期2026-09-25
產品代碼QIH
諮詢委員會RA
決定Substantially Equivalent

器材摘要

syngo.CT Brain Quantification 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 2026-09-25 under 510(k) number K260055. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the syngo.CT Brain Quantification?

syngo.CT Brain Quantification is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K260055.

When did syngo.CT Brain Quantification receive FDA 510(k) clearance?

syngo.CT Brain Quantification received FDA 510(k) clearance on 2026-09-25, under 510(k) number K260055.

Who is the listed applicant for syngo.CT Brain Quantification?

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 syngo.CT Brain Quantification?

The FDA product code for syngo.CT Brain Quantification is QIH.

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

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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相關器械（代碼：QIH）

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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