FDA 510(k)

HI-TORQUE TurnTrac 引導絲線系列

K 號：K173795 · 2018-01-12

決定日期2018-01-12

產品代碼DQX

諮詢委員會履歷

決定相當於

器材摘要

HI-TORQUE TurnTrac Guide Wire Family is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Vascular. It received FDA 510(k) clearance on 2018-01-12 under 510(k) number K173795. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the HI-TORQUE TurnTrac Guide Wire Family?

HI-TORQUE TurnTrac Guide Wire Family is a medical device that received FDA 510(k) clearance on 2018-01-12. The listed applicant is Abbott Vascular. The 510(k) number is K173795.

When did HI-TORQUE TurnTrac Guide Wire Family receive FDA 510(k) clearance?

HI-TORQUE TurnTrac Guide Wire Family received FDA 510(k) clearance on 2018-01-12, under 510(k) number K173795.

Who is the listed applicant for HI-TORQUE TurnTrac Guide Wire Family?

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

What is the FDA product code for HI-TORQUE TurnTrac Guide Wire Family?

The FDA product code for HI-TORQUE TurnTrac Guide Wire Family is DQX.

其他以 Abbott Vascular 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。

K220634NC TREK NEO 冠狀擴張導管 K221057Viatrac 14 Plus 頸動脈擴張針管 K201834HI-TORQUE PROCEED 線導管系列 K200144高扭矩鋼芯裸導引絲 K193126HI-TORQUE InfilTrac 導引絲系列 K191173Emboshield NAV6 體內栓子防護系統，裸線過濾導線

查看所有 11 項裝置 →

相關器械（代碼：DQX）

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。

K253146超驅35導絲Rapid-Medical , Ltd.K261281CROSSLEAD 标準 035 和 CROSSLEAD 硬度 035Filmecc Co., Ltd.K253667Accoat 引導絲Sp Medical A/S K261640優質美克硝化鋼/金-鎳合金導引絲Merit Medical Ireland , Ltd.K254137InQwire Amplatz 引導絲Merit Medical Ireland, Ltd.K260544FMD周邊導引絲F-14柔軟6；FMD周邊導引絲F-14緩坡40；FMD周邊導引絲F-18柔軟SP；FMD周邊導引絲F-18 DP 25；FMD周邊導引絲F-18緩坡40FMD Co., Ltd.

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。