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FDA 510(k)

科德曼Libertís分流針管搭配Bactiseal及Endexo技術

K 號:K243531 · 2025-08-08

決定日期2025-08-08
產品代碼JXG
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology is the device name listed in this FDA 510(k) record. The listed applicant is Integra Lifesciences Production Corporation. It received FDA 510(k) clearance on 2025-08-08 under 510(k) number K243531. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology?

Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology is a medical device that received FDA 510(k) clearance on 2025-08-08. The listed applicant is Integra Lifesciences Production Corporation. The 510(k) number is K243531.

When did Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology receive FDA 510(k) clearance?

Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology received FDA 510(k) clearance on 2025-08-08, under 510(k) number K243531.

Who is the listed applicant for Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology?

The FDA 510(k) record lists Integra Lifesciences Production Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology?

The FDA product code for Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology is JXG.

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其他以 Integra Lifesciences Production Corporation 為申請人之記錄

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相關器械(代碼:JXG)

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。

官方來源

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