NovoFlow 加強型輸尿管支架
K 號：K213186 · 2022-02-16
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器材摘要
NovoFlow Reinforced Ureteral Stent is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast Corp.. It received FDA 510(k) clearance on 2022-02-16 under 510(k) number K213186. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常見問題
What is the NovoFlow Reinforced Ureteral Stent?
NovoFlow Reinforced Ureteral Stent is a medical device that received FDA 510(k) clearance on 2022-02-16. The listed applicant is Coloplast Corp.. The 510(k) number is K213186.
When did NovoFlow Reinforced Ureteral Stent receive FDA 510(k) clearance?
NovoFlow Reinforced Ureteral Stent received FDA 510(k) clearance on 2022-02-16, under 510(k) number K213186.
Who is the listed applicant for NovoFlow Reinforced Ureteral Stent?
The FDA 510(k) record lists Coloplast Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NovoFlow Reinforced Ureteral Stent?
The FDA product code for NovoFlow Reinforced Ureteral Stent is FAD.
相關臨床試驗
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其他以 Coloplast Corp. 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：FAD）
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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