PureLift Pro 版本
K 號：K230506 · 2023-06-21
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器材摘要
PureLift Pro Edition is the device name listed in this FDA 510(k) record. The listed applicant is Xtreem Pulse. It received FDA 510(k) clearance on 2023-06-21 under 510(k) number K230506. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PureLift Pro Edition?
PureLift Pro Edition is a medical device that received FDA 510(k) clearance on 2023-06-21. The listed applicant is Xtreem Pulse. The 510(k) number is K230506.
When did PureLift Pro Edition receive FDA 510(k) clearance?
PureLift Pro Edition received FDA 510(k) clearance on 2023-06-21, under 510(k) number K230506.
Who is the listed applicant for PureLift Pro Edition?
The FDA 510(k) record lists Xtreem Pulse as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PureLift Pro Edition?
The FDA product code for PureLift Pro Edition is NFO.
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：NFO）
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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