AirFit F30i 面罩系統; AirFit F30i NM 面罩系統; Arcadia 面罩系統
K 號:K234134 · 2024-09-24
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器材摘要
常見問題
What is the AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System?
AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System is a medical device that received FDA 510(k) clearance on 2024-09-24. The listed applicant is Resmed Pty Ltd (Registration Number: 3004604967). The 510(k) number is K234134.
When did AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System receive FDA 510(k) clearance?
AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System received FDA 510(k) clearance on 2024-09-24, under 510(k) number K234134.
Who is the listed applicant for AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System?
The FDA 510(k) record lists Resmed Pty Ltd (Registration Number: 3004604967) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System?
The FDA product code for AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System is BZD.
相關臨床試驗
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其他以 Resmed Pty Ltd (Registration Number: 3004604967) 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。
相關器械(代碼:BZD)
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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