Inzii Ripstop 可重部署回收系統
K 號：K232880 · 2023-11-01
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器材摘要
常見問題
What is the Inzii Ripstop Redeployable Retrieval System?
Inzii Ripstop Redeployable Retrieval System is a medical device that received FDA 510(k) clearance on 2023-11-01. The listed applicant is Applied Medical Resources Corporation. The 510(k) number is K232880.
When did Inzii Ripstop Redeployable Retrieval System receive FDA 510(k) clearance?
Inzii Ripstop Redeployable Retrieval System received FDA 510(k) clearance on 2023-11-01, under 510(k) number K232880.
Who is the listed applicant for Inzii Ripstop Redeployable Retrieval System?
The FDA 510(k) record lists Applied Medical Resources Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Inzii Ripstop Redeployable Retrieval System?
The FDA product code for Inzii Ripstop Redeployable Retrieval System 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 Applied Medical Resources 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。
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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