Xpan 選擇式內視鏡手術系統
K 號：K223562 · 2023-06-02
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器材摘要
Xpan Universal Trocar System is the device name listed in this FDA 510(k) record. The listed applicant is Xpan, Inc.. It received FDA 510(k) clearance on 2023-06-02 under 510(k) number K223562. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Xpan Universal Trocar System?
Xpan Universal Trocar System is a medical device that received FDA 510(k) clearance on 2023-06-02. The listed applicant is Xpan, Inc.. The 510(k) number is K223562.
When did Xpan Universal Trocar System receive FDA 510(k) clearance?
Xpan Universal Trocar System received FDA 510(k) clearance on 2023-06-02, under 510(k) number K223562.
Who is the listed applicant for Xpan Universal Trocar System?
The FDA 510(k) record lists Xpan, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Xpan Universal Trocar System?
The FDA product code for Xpan Universal Trocar System is GCJ.
相關臨床試驗
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相關器械（代碼：GCJ）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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