Inno-Port 一次性刀片型穿刺器
K 號：K252532 · 2026-06-02
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器材摘要
Inno-Port Disposable Bladed Trocar is the device name listed in this FDA 510(k) record. The listed applicant is Taiwan Surgical Corporation. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K252532. 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 Inno-Port Disposable Bladed Trocar?
Inno-Port Disposable Bladed Trocar is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is Taiwan Surgical Corporation. The 510(k) number is K252532.
When did Inno-Port Disposable Bladed Trocar receive FDA 510(k) clearance?
Inno-Port Disposable Bladed Trocar received FDA 510(k) clearance on 2026-06-02, under 510(k) number K252532.
Who is the listed applicant for Inno-Port Disposable Bladed Trocar?
FDA 510(k) 記錄中將台灣外科股份有限公司列為申請人。這並不單獨確立設備製造商的身份。
What is the FDA product code for Inno-Port Disposable Bladed Trocar?
The FDA product code for Inno-Port Disposable Bladed Trocar is GCJ.
相關臨床試驗
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。
其他以 Taiwan Surgical Corporation 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。
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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