PliaFX Flo
K 號：K242799 · 2024-11-21
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器材摘要
PliaFX Flo is the device name listed in this FDA 510(k) record. The listed applicant is Lifenet Health. It received FDA 510(k) clearance on 2024-11-21 under 510(k) number K242799. The device is classified under product code MBP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PliaFX Flo?
PliaFX Flo is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is Lifenet Health. The 510(k) number is K242799.
When did PliaFX Flo receive FDA 510(k) clearance?
PliaFX Flo received FDA 510(k) clearance on 2024-11-21, under 510(k) number K242799.
Who is the listed applicant for PliaFX Flo?
The FDA 510(k) record lists Lifenet Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PliaFX Flo?
The FDA product code for PliaFX Flo is MBP.
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其他以 Lifenet Health 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。
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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