FDA 510(k)

安全導絲導管

K 號：K180756 · 2018-05-24

決定日期2018-05-24

產品代碼EZN

諮詢委員會GU

決定相當於

器材摘要

Safety Wire Guide Introducer is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2018-05-24 under 510(k) number K180756. The device is classified under product code EZN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Safety Wire Guide Introducer?

Safety Wire Guide Introducer is a medical device that received FDA 510(k) clearance on 2018-05-24. The listed applicant is Cook Incorporated. The 510(k) number is K180756.

When did Safety Wire Guide Introducer receive FDA 510(k) clearance?

Safety Wire Guide Introducer received FDA 510(k) clearance on 2018-05-24, under 510(k) number K180756.

Who is the listed applicant for Safety Wire Guide Introducer?

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

What is the FDA product code for Safety Wire Guide Introducer?

The FDA product code for Safety Wire Guide Introducer is EZN.

其他以 Cook Incorporated 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：EZN）

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。

K250910Optilume® 高壓泌尿學氣球擴張導尿管Urotronic, Inc.K220781ARMADA Ureteral Dilator Set, ARMADA Nottingham One Step Dilator, ARMADA Amplatz Renal Dilator Sets, ARMADA Renal Dilator, Glider Amplatz Sheath, ARMADA Renal Dilator with Amplatz Sheath, Fascial Dilator Set, Introducer Sheath, Introducer CatheterAllwin Medical Devices, Inc.K201007In-Ka 腎管氣球擴張針管Coloplast Corp.K190612EQUINOX 气球擴張導管Dornier Medtech America, Inc.K173654輸尿管擴張器組合，輸尿管擴張器Cook Incorporated K180028Cook 810 設備組，Desilets-Hoffman 引導器組Cook Incorporated

官方來源

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