福吉蒂螺旋导管;福吉蒂移植物血栓切除导管
K 號:K233619 · 2024-05-20
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器材摘要
常見問題
What is the Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters?
Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters is a medical device that received FDA 510(k) clearance on 2024-05-20. The listed applicant is Edwards Lifesciences. The 510(k) number is K233619.
When did Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters receive FDA 510(k) clearance?
Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters received FDA 510(k) clearance on 2024-05-20, under 510(k) number K233619.
Who is the listed applicant for Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters?
The FDA 510(k) record lists Edwards Lifesciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters?
The FDA product code for Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters is DXE.
相關臨床試驗
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其他以 Edwards Lifesciences 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:DXE)
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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