FDA 510(k)

somatom Scope（配備 syngo CT VC30-easyIQ 版本），SOMATOM Scope Power（配備 syngo CT VC30-easyIQ 版本）

K 號：K151749 · 2016-03-18

決定日期2016-03-18

產品代碼JAK

諮詢委員會RA

決定相當於

器材摘要

somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version) 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 2016-03-18 under 510(k) number K151749. 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 Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version)?

somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version) is a medical device that received FDA 510(k) clearance on 2016-03-18. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K151749.

When did somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version) receive FDA 510(k) clearance?

somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version) received FDA 510(k) clearance on 2016-03-18, under 510(k) number K151749.

Who is the listed applicant for somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version)?

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 somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version)?

The FDA product code for somatom Scope(with syngo CT VC30-easyIQ version), SOMATOM Scope Power(with syngo CT VC30-easyIQ version) is JAK.

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：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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