FDA 510(k)

CEREGLIDE 92 管道系統

K 號：K233982 · 2024-05-09

決定日期2024-05-09

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

CEREGLIDE 92 Catheter System is the device name listed in this FDA 510(k) record. The listed applicant is Cerenovus, Inc.. It received FDA 510(k) clearance on 2024-05-09 under 510(k) number K233982. 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 92 Catheter System?

CEREGLIDE 92 Catheter System is a medical device that received FDA 510(k) clearance on 2024-05-09. The listed applicant is Cerenovus, Inc.. The 510(k) number is K233982.

When did CEREGLIDE 92 Catheter System receive FDA 510(k) clearance?

CEREGLIDE 92 Catheter System received FDA 510(k) clearance on 2024-05-09, under 510(k) number K233982.

Who is the listed applicant for CEREGLIDE 92 Catheter System?

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 92 Catheter System?

The FDA product code for CEREGLIDE 92 Catheter System 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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