FDA 510(k)

X-Suit 近紅外線肝內金屬支架

K 號：K150487 · 2016-02-12

決定日期2016-02-12

產品代碼FGE

諮詢委員會GU

決定Unknown

器材摘要

X-Suit NIR Biliary Metallic Stent is the device name listed in this FDA 510(k) record. The listed applicant is Medinol, Ltd.. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K150487. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常見問題

What is the X-Suit NIR Biliary Metallic Stent?

X-Suit NIR Biliary Metallic Stent is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Medinol, Ltd.. The 510(k) number is K150487.

When did X-Suit NIR Biliary Metallic Stent receive FDA 510(k) clearance?

X-Suit NIR Biliary Metallic Stent received FDA 510(k) clearance on 2016-02-12, under 510(k) number K150487.

Who is the listed applicant for X-Suit NIR Biliary Metallic Stent?

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

What is the FDA product code for X-Suit NIR Biliary Metallic Stent?

The FDA product code for X-Suit NIR Biliary Metallic Stent is FGE.

其他以 Medinol, Ltd. 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。

K173581英勇PTCA擴張針管 K162434NC Gallant PTCA 球囊导管

相關器械（代碼：FGE）

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。

K254179引流針管Canyon Medical, Inc.K262913Protégé™ EverFlex™ 自擴張週邊支架系統Medtronic, Inc.K260835阿基米德可生物降解支架（中號）Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.)K253393單次使用氣球擴張導管（AG-5251-083018 AG-5251-085518 AG-5251-088018 AG-5251-083019 AG-5251-085519 AG-5251-088019 AG-5251-083021 AG-5251-085521 AG-5251-088021 AG-5251-083024 AG-5251-085524 AG-5251-088024 AG-5251-103018 AG-5251-105518 AG-5251-108018 AG-5251-103019 AG-5251-105519 AG-5251-108019 AG-5251-103021 AG-5251-105521 AG-5251-108021 AG-5251-103024 AG-5251-105524 AG-5251-108024 AG-5251-123018 AG-5251-125518 AG-5251-128018 AG-5251-123019 AG-5251-125519 AG-5251-128019）Hangzhou AGS MedTech Co., Ltd.K253832擴張氣球心导管Mirco-Tech (Nanjing) Co., Ltd.K251658Endoflux™ 胆胰支架組Medi-Globe GmbH

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。