FDA 510(k)

大腦自調節指數（CAI）算法

K 號：K240596 · 2024-10-16

決定日期2024-10-16

產品代碼MUD

諮詢委員會履歷

決定相當於

器材摘要

Cerebral Autoregulation Index (CAI) Algorithm is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lifesciences. It received FDA 510(k) clearance on 2024-10-16 under 510(k) number K240596. The device is classified under product code MUD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cerebral Autoregulation Index (CAI) Algorithm?

Cerebral Autoregulation Index (CAI) Algorithm is a medical device that received FDA 510(k) clearance on 2024-10-16. The listed applicant is Edwards Lifesciences. The 510(k) number is K240596.

When did Cerebral Autoregulation Index (CAI) Algorithm receive FDA 510(k) clearance?

Cerebral Autoregulation Index (CAI) Algorithm received FDA 510(k) clearance on 2024-10-16, under 510(k) number K240596.

Who is the listed applicant for Cerebral Autoregulation Index (CAI) Algorithm?

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

What is the FDA product code for Cerebral Autoregulation Index (CAI) Algorithm?

The FDA product code for Cerebral Autoregulation Index (CAI) Algorithm is MUD.

其他以 Edwards Lifesciences 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：MUD）

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。

K254129Spectrum-2Neko Health AB K243324馬斯米O3地區性血氧儀Masimo Corporation K250519Lap.Ox™ 鍋鏡組織氧濃度計ViOptix, Inc.K241393ODI-TechOdi Medical AS K240601快照NIR型 KD205Kent Imaging, Inc.K232385OxiplexTS200Iss Medical, Inc.

官方來源

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