FDA 510(k)

CEREGLIDE 42 中間導管；CEREGLIDE 57 中間導管

K 號：K241244 · 2024-10-16

決定日期2024-10-16

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Cerenovus, Inc.. It received FDA 510(k) clearance on 2024-10-16 under 510(k) number K241244. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter?

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter is a medical device that received FDA 510(k) clearance on 2024-10-16. The listed applicant is Cerenovus, Inc.. The 510(k) number is K241244.

When did CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter receive FDA 510(k) clearance?

CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter received FDA 510(k) clearance on 2024-10-16, under 510(k) number K241244.

Who is the listed applicant for CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter?

FDA 510(k) 記錄將 Cerenovus, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter?

The FDA product code for CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter is QJP.

其他以 Cerenovus, Inc. 為申請人之記錄

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相關器械（代碼：QJP）

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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