FDA 510(k)

一步式會陰導入器

K 號：K182709 · 2018-12-26

決定日期2018-12-26

產品代碼KOB

諮詢委員會GU

決定相當於

器材摘要

One-Step Suprapubic 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 2018-12-26 under 510(k) number K182709. The device is classified under product code KOB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the One-Step Suprapubic Introducer?

One-Step Suprapubic Introducer is a medical device that received FDA 510(k) clearance on 2018-12-26. The listed applicant is Cook Incorporated. The 510(k) number is K182709.

When did One-Step Suprapubic Introducer receive FDA 510(k) clearance?

One-Step Suprapubic Introducer received FDA 510(k) clearance on 2018-12-26, under 510(k) number K182709.

Who is the listed applicant for One-Step Suprapubic 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 One-Step Suprapubic Introducer?

The FDA product code for One-Step Suprapubic Introducer is KOB.

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：KOB）

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。

K240514AMT 低輪廓會陰導尿管與引流套件Applied Medical Technology, Inc.K181097庫克膀胱造口導尿管組合Cook Incorporated K182066歐布萊恩超聽導管設備組，庫克SP管導管設備組Cook Incorporated

官方來源

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