iPhyso® 系統
K 號：K232383 · 2025-03-04
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器材摘要
iPhysio® System is the device name listed in this FDA 510(k) record. The listed applicant is Euroteknika. It received FDA 510(k) clearance on 2025-03-04 under 510(k) number K232383. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the iPhysio® System?
iPhysio® System is a medical device that received FDA 510(k) clearance on 2025-03-04. The listed applicant is Euroteknika. The 510(k) number is K232383.
When did iPhysio® System receive FDA 510(k) clearance?
iPhysio® System received FDA 510(k) clearance on 2025-03-04, under 510(k) number K232383.
Who is the listed applicant for iPhysio® System?
The FDA 510(k) record lists Euroteknika as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iPhysio® System?
The FDA product code for iPhysio® System is NHA.
相關臨床試驗
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相關器械（代碼：NHA）
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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