Ellipsys血管通路系統(Ellipsys系統),(功率控制器型號AMi-1001及導管與針型號AMi-6005)
K 號:K181725 · 2018-10-05
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器材摘要
常見問題
What is the Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005)?
Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005) is a medical device that received FDA 510(k) clearance on 2018-10-05. The listed applicant is Avenu Medical, Inc.. The 510(k) number is K181725.
When did Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005) receive FDA 510(k) clearance?
Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005) received FDA 510(k) clearance on 2018-10-05, under 510(k) number K181725.
Who is the listed applicant for Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005)?
The FDA 510(k) record lists Avenu Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005)?
The FDA product code for Ellipsys Vascular Access System (Ellipsys System), (Power Controller Model No. AMI-1001 & Catheter & Needle Model No. AMI-6005) is PQK.
相關臨床試驗
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其他以 Avenu Medical, Inc. 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:PQK)
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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