FDA 510(k)

Fogg 系統病人監護電纜

K 號：K222712 · 2023-11-22

決定日期2023-11-22

產品代碼DSA

諮詢委員會履歷

決定相當於

器材摘要

Fogg System Patient Monitoring Cables is the device name listed in this FDA 510(k) record. The listed applicant is Fogg System Company, Inc.. It received FDA 510(k) clearance on 2023-11-22 under 510(k) number K222712. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Fogg System Patient Monitoring Cables?

Fogg System Patient Monitoring Cables is a medical device that received FDA 510(k) clearance on 2023-11-22. The listed applicant is Fogg System Company, Inc.. The 510(k) number is K222712.

When did Fogg System Patient Monitoring Cables receive FDA 510(k) clearance?

Fogg System Patient Monitoring Cables received FDA 510(k) clearance on 2023-11-22, under 510(k) number K222712.

Who is the listed applicant for Fogg System Patient Monitoring Cables?

The FDA 510(k) record lists Fogg System Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fogg System Patient Monitoring Cables?

The FDA product code for Fogg System Patient Monitoring Cables is DSA.

相關器械（代碼：DSA）

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：DSA）

官方來源