FDA 510(k)

Glidewire GT

K 號：K170417 · 2017-09-15

決定日期2017-09-15

產品代碼DQX

諮詢委員會履歷

決定相當於

器材摘要

Glidewire GT is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Corporation. It received FDA 510(k) clearance on 2017-09-15 under 510(k) number K170417. 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 Glidewire GT?

Glidewire GT is a medical device that received FDA 510(k) clearance on 2017-09-15. The listed applicant is Terumo Corporation. The 510(k) number is K170417.

When did Glidewire GT receive FDA 510(k) clearance?

Glidewire GT received FDA 510(k) clearance on 2017-09-15, under 510(k) number K170417.

Who is the listed applicant for Glidewire GT?

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

What is the FDA product code for Glidewire GT?

The FDA product code for Glidewire GT is DQX.

其他以 Terumo Corporation 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：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

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