Active System; Avenue8
K 號：K241395 · 2024-12-18
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器材摘要
Active System; Avenue8 is the device name listed in this FDA 510(k) record. The listed applicant is Caerus Corporation. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K241395. The device is classified under product code ILX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Active System; Avenue8?
Active System; Avenue8 is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Caerus Corporation. The 510(k) number is K241395.
When did Active System; Avenue8 receive FDA 510(k) clearance?
Active System; Avenue8 received FDA 510(k) clearance on 2024-12-18, under 510(k) number K241395.
Who is the listed applicant for Active System; Avenue8?
The FDA 510(k) record lists Caerus Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Active System; Avenue8?
The FDA product code for Active System; Avenue8 is ILX.
相關臨床試驗
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相關器械（代碼：ILX）
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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