空气压缩腿部按摩器（型号：EMK-701）
K 號：K222991 · 2023-03-15
廣告
器材摘要
常見問題
What is the Air Compression Leg Massager (model: EMK-701)?
Air Compression Leg Massager (model: EMK-701) is a medical device that received FDA 510(k) clearance on 2023-03-15. The listed applicant is Xiamen Emoka Health Science & Technology Co., Ltd.. The 510(k) number is K222991.
When did Air Compression Leg Massager (model: EMK-701) receive FDA 510(k) clearance?
Air Compression Leg Massager (model: EMK-701) received FDA 510(k) clearance on 2023-03-15, under 510(k) number K222991.
Who is the listed applicant for Air Compression Leg Massager (model: EMK-701)?
The FDA 510(k) record lists Xiamen Emoka Health Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Compression Leg Massager (model: EMK-701)?
The FDA product code for Air Compression Leg Massager (model: EMK-701) 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。
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