FDA 510(k)

CEREGLIDE 71 中間導管

K 號：K221930 · 2023-03-09

決定日期2023-03-09

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

CEREGLIDE 71 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 2023-03-09 under 510(k) number K221930. 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 71 Intermediate Catheter?

CEREGLIDE 71 Intermediate Catheter is a medical device that received FDA 510(k) clearance on 2023-03-09. The listed applicant is Cerenovus, Inc.. The 510(k) number is K221930.

When did CEREGLIDE 71 Intermediate Catheter receive FDA 510(k) clearance?

CEREGLIDE 71 Intermediate Catheter received FDA 510(k) clearance on 2023-03-09, under 510(k) number K221930.

Who is the listed applicant for CEREGLIDE 71 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 71 Intermediate Catheter?

The FDA product code for CEREGLIDE 71 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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