預測健康體成分
K 號：K242825 · 2025-01-17
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器材摘要
Prenuvo Body Composition is the device name listed in this FDA 510(k) record. The listed applicant is Prenuvo. It received FDA 510(k) clearance on 2025-01-17 under 510(k) number K242825. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Prenuvo Body Composition?
Prenuvo Body Composition is a medical device that received FDA 510(k) clearance on 2025-01-17. The listed applicant is Prenuvo. The 510(k) number is K242825.
When did Prenuvo Body Composition receive FDA 510(k) clearance?
Prenuvo Body Composition received FDA 510(k) clearance on 2025-01-17, under 510(k) number K242825.
Who is the listed applicant for Prenuvo Body Composition?
The FDA 510(k) record lists Prenuvo as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prenuvo Body Composition?
The FDA product code for Prenuvo Body Composition is LNH.
相關臨床試驗
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相關器械（代碼：LNH）
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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