腿部及足部氣波壓力治療設備
K 號：K223464 · 2023-03-14
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器材摘要
Leg and Foot Air Wave Pressure Therapy Device is the device name listed in this FDA 510(k) record. The listed applicant is Zhangzhou Easepal Innovation CO , Ltd.. It received FDA 510(k) clearance on 2023-03-14 under 510(k) number K223464. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Leg and Foot Air Wave Pressure Therapy Device?
Leg and Foot Air Wave Pressure Therapy Device is a medical device that received FDA 510(k) clearance on 2023-03-14. The listed applicant is Zhangzhou Easepal Innovation CO , Ltd.. The 510(k) number is K223464.
When did Leg and Foot Air Wave Pressure Therapy Device receive FDA 510(k) clearance?
Leg and Foot Air Wave Pressure Therapy Device received FDA 510(k) clearance on 2023-03-14, under 510(k) number K223464.
Who is the listed applicant for Leg and Foot Air Wave Pressure Therapy Device?
The FDA 510(k) record lists Zhangzhou Easepal Innovation CO , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Leg and Foot Air Wave Pressure Therapy Device?
The FDA product code for Leg and Foot Air Wave Pressure Therapy Device is IRP.
相關臨床試驗
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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。
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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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