FDA 510(k)

魯士間歇性尿道導尿管

K 號：K173596 · 2018-01-29

決定日期2018-01-29

產品代碼EZC

諮詢委員會GU

決定相當於

器材摘要

Rusch Intermittent Urethral Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2018-01-29 under 510(k) number K173596. The device is classified under product code EZC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Rusch Intermittent Urethral Catheters?

Rusch Intermittent Urethral Catheters is a medical device that received FDA 510(k) clearance on 2018-01-29. The listed applicant is Teleflex Medical. The 510(k) number is K173596.

When did Rusch Intermittent Urethral Catheters receive FDA 510(k) clearance?

Rusch Intermittent Urethral Catheters received FDA 510(k) clearance on 2018-01-29, under 510(k) number K173596.

Who is the listed applicant for Rusch Intermittent Urethral Catheters?

FDA 510(k) 記錄將Teleflex Medical列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for Rusch Intermittent Urethral Catheters?

The FDA product code for Rusch Intermittent Urethral Catheters is EZC.

其他以 Teleflex Medical 為申請人之記錄

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相關器械（代碼：EZC）

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。

K222279魯士間歇性尿道導尿管Teleflex Medical

官方來源

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