無刀針 Trocar – 阿瑞斯 Lap 穿刺針
K 號：K230058 · 2023-04-28
廣告
器材摘要
Bladeless Trocar – Artemis Lap Cannula is the device name listed in this FDA 510(k) record. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. It received FDA 510(k) clearance on 2023-04-28 under 510(k) number K230058. 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 Bladeless Trocar – Artemis Lap Cannula?
Bladeless Trocar – Artemis Lap Cannula is a medical device that received FDA 510(k) clearance on 2023-04-28. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. The 510(k) number is K230058.
When did Bladeless Trocar – Artemis Lap Cannula receive FDA 510(k) clearance?
Bladeless Trocar – Artemis Lap Cannula received FDA 510(k) clearance on 2023-04-28, under 510(k) number K230058.
Who is the listed applicant for Bladeless Trocar – Artemis Lap Cannula?
FDA 510(k) 記錄將 T.A.G. 医療產品股份有限公司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 Bladeless Trocar – Artemis Lap Cannula?
The FDA product code for Bladeless Trocar – Artemis Lap Cannula 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 T.A.G. Medical Products Corporation, Ltd. 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。
K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE選擇系統Karl Storz SE & CO. KGK260972OEV-271MUH LCD 螢幕；OEV-321MUH LCD 螢幕；OEV-431MUH LCD 螢幕Sony CorporationK261139VereSee (VER150、VER200、VER151、VER201、VER200C 及 VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™（EZ Close Port Site Closing Device、EZ Close MAX Port Site Closing Device、EZ Close II Port Site Closing Device）Medical ImpactK261614LED LCD 螢幕 (OEV-271H)Lg Electronics.Inc
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。
廣告