FDA 510(k)

IRRAflow 活動濾液交換系統 (AFES)

K 號：K231664 · 2023-10-19

決定日期2023-10-19

產品代碼JXG

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

IRRAflow Active Fluid Exchange System (AFES) is the device name listed in this FDA 510(k) record. The listed applicant is Irras USA, Inc.. It received FDA 510(k) clearance on 2023-10-19 under 510(k) number K231664. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the IRRAflow Active Fluid Exchange System (AFES)?

IRRAflow Active Fluid Exchange System (AFES) is a medical device that received FDA 510(k) clearance on 2023-10-19. The listed applicant is Irras USA, Inc.. The 510(k) number is K231664.

When did IRRAflow Active Fluid Exchange System (AFES) receive FDA 510(k) clearance?

IRRAflow Active Fluid Exchange System (AFES) received FDA 510(k) clearance on 2023-10-19, under 510(k) number K231664.

Who is the listed applicant for IRRAflow Active Fluid Exchange System (AFES)?

The FDA 510(k) record lists Irras USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IRRAflow Active Fluid Exchange System (AFES)?

The FDA product code for IRRAflow Active Fluid Exchange System (AFES) is JXG.

其他以 Irras USA, 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。

K200807IRRAflow 管腔導管，IRRAflow 管道組，IRRAflow 控制單元

相關器械（代碼：JXG）

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。

K261004Codman® 遠端腹膜針管，铍白開口型（82-1682）；Codman® HOLTER® 腹膜針管（SALMON設計）（82-1684）Integra Lifesciences Production Corporation K251598智滴Brainspace, Inc.K250636Sophy Mini 單壓力閥 (SM1)Sophysa K252514EVAC-MRIPhasor Health, LLC K243531科德曼Libertís分流針管搭配Bactiseal及Endexo技術Integra Lifesciences Production Corporation K243552Codman Libertís™ 1.5 mm EVD 腔管，配備 Bactiseal® 及 Endexo® 技術，並具有 Luer 接頭（821761）；Codman Libertís™ 1.9 mm EVD 腔管，配備 Bactiseal® 及 Endexo® 技術，並具有 Luer 接頭（821762）Integra Lifesciences Production Corporation

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。