FDA 510(k)

KIDNEYvault 過濾式腎灌流系統

K 號：K234060 · 2024-10-23

決定日期2024-10-23

產品代碼KDN

諮詢委員會GU

決定相當於

器材摘要

KIDNEYvault Portable Renal Perfusion System is the device name listed in this FDA 510(k) record. The listed applicant is Paragonix Technologies. It received FDA 510(k) clearance on 2024-10-23 under 510(k) number K234060. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the KIDNEYvault Portable Renal Perfusion System?

KIDNEYvault Portable Renal Perfusion System is a medical device that received FDA 510(k) clearance on 2024-10-23. The listed applicant is Paragonix Technologies. The 510(k) number is K234060.

When did KIDNEYvault Portable Renal Perfusion System receive FDA 510(k) clearance?

KIDNEYvault Portable Renal Perfusion System received FDA 510(k) clearance on 2024-10-23, under 510(k) number K234060.

Who is the listed applicant for KIDNEYvault Portable Renal Perfusion System?

The FDA 510(k) record lists Paragonix Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIDNEYvault Portable Renal Perfusion System?

The FDA product code for KIDNEYvault Portable Renal Perfusion System is KDN.

其他以 Paragonix Technologies 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。

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相關器械（代碼：KDN）

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。

K261644Perfadex PlusXvivo Perfusion AB K260456VI°Port™ 肝臟保存系統Traferox Technologies, Inc.K254305BAROguard 腎臟捐贈保存系統Paragonix Technologies, Inc.K243618EasiSlush® 食鹽溶液，用於無菌冰沙製備 (BTLE-1250)Bridge TO Life K243870X°Port 肺部保存系統；X°Port 肺部保存解決方案Traferox Technologies, Inc.K243998DCX一次性卡式碟 (DCX)Institut Geroges Lopez

官方來源

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