Air Relax Plus 型號 AR-3.0
K 號：K211460 · 2021-05-25
廣告
器材摘要
常見問題
What is the Air Relax Plus Model AR-3.0?
Air Relax Plus Model AR-3.0 is a medical device that received FDA 510(k) clearance on 2021-05-25. The listed applicant is Diode Art Engineering Doing Business AS Air Relax. The 510(k) number is K211460.
When did Air Relax Plus Model AR-3.0 receive FDA 510(k) clearance?
Air Relax Plus Model AR-3.0 received FDA 510(k) clearance on 2021-05-25, under 510(k) number K211460.
Who is the listed applicant for Air Relax Plus Model AR-3.0?
The FDA 510(k) record lists Diode Art Engineering Doing Business AS Air Relax as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Relax Plus Model AR-3.0?
The FDA product code for Air Relax Plus Model AR-3.0 is IRP.
相關臨床試驗
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。
其他以 Diode Art Engineering Doing Business AS Air Relax 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：IRP）
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。
廣告