FDA 510(k)

益康乳膠福爾氏導尿管

K 號：K173340 · 2018-07-13

申請人Jiangxi Yikang Medical Instrument Group Co., Ltd.

決定日期2018-07-13

產品代碼EZL

諮詢委員會GU

決定相當於

器材摘要

Yikang Latex Foley Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Jiangxi Yikang Medical Instrument Group Co., Ltd.. It received FDA 510(k) clearance on 2018-07-13 under 510(k) number K173340. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Yikang Latex Foley Catheter?

Yikang Latex Foley Catheter is a medical device that received FDA 510(k) clearance on 2018-07-13. The listed applicant is Jiangxi Yikang Medical Instrument Group Co., Ltd.. The 510(k) number is K173340.

When did Yikang Latex Foley Catheter receive FDA 510(k) clearance?

Yikang Latex Foley Catheter received FDA 510(k) clearance on 2018-07-13, under 510(k) number K173340.

Who is the listed applicant for Yikang Latex Foley Catheter?

The FDA 510(k) record lists Jiangxi Yikang Medical Instrument Group Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Yikang Latex Foley Catheter?

The FDA product code for Yikang Latex Foley Catheter is EZL.

其他以 Jiangxi Yikang Medical Instrument Group Co., 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。

K190213益康內氣管管

相關器械（代碼：EZL）

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。

K260756TraumaGuard 腹腔內壓力感知系統 (000-0221)Sentinel Medical Technologies,K262056魯士拉特克斯金福樓伊姆導尿管Teleflex Medical Sdn. Bhd.K252537魯士軟簡塑福樸利氧導管Teleflex Medical Sdn. Bhd.K243011矽膠尿道導尿管（矽膠尿道導尿管）Guangdong Ecan Medical Co., Ltd.K241424InnoCare 專業福爾伊灌腸器Innocare Urologics, LLC K232469魯施天然乳膠金屬福樸導尿管Teleflexmedical, Inc.

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。