FDA 510(k)

Cordis BRITECROSS 支援導管

K 號：K233637 · 2024-06-28

決定日期2024-06-28

產品代碼DQY

諮詢委員會履歷

決定相當於

器材摘要

Cordis BRITECROSS Support Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Cordis US Corp. It received FDA 510(k) clearance on 2024-06-28 under 510(k) number K233637. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cordis BRITECROSS Support Catheter?

Cordis BRITECROSS Support Catheter is a medical device that received FDA 510(k) clearance on 2024-06-28. The listed applicant is Cordis US Corp. The 510(k) number is K233637.

When did Cordis BRITECROSS Support Catheter receive FDA 510(k) clearance?

Cordis BRITECROSS Support Catheter received FDA 510(k) clearance on 2024-06-28, under 510(k) number K233637.

Who is the listed applicant for Cordis BRITECROSS Support Catheter?

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

What is the FDA product code for Cordis BRITECROSS Support Catheter?

The FDA product code for Cordis BRITECROSS Support Catheter is DQY.

其他以 Cordis US Corp 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：DQY）

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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官方來源

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