AMP by Method Mobility, AMP Plus (or +) by Method Mobility
K 號:K231032 · 2023-05-10
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器材摘要
常見問題
What is the AMP by Method Mobility, AMP Plus (or +) by Method Mobility?
AMP by Method Mobility, AMP Plus (or +) by Method Mobility is a medical device that received FDA 510(k) clearance on 2023-05-10. The listed applicant is Method Mobility. The 510(k) number is K231032.
When did AMP by Method Mobility, AMP Plus (or +) by Method Mobility receive FDA 510(k) clearance?
AMP by Method Mobility, AMP Plus (or +) by Method Mobility received FDA 510(k) clearance on 2023-05-10, under 510(k) number K231032.
Who is the listed applicant for AMP by Method Mobility, AMP Plus (or +) by Method Mobility?
The FDA 510(k) record lists Method Mobility as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMP by Method Mobility, AMP Plus (or +) by Method Mobility?
The FDA product code for AMP by Method Mobility, AMP Plus (or +) by Method Mobility is ITI.
相關臨床試驗
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相關器械(代碼:ITI)
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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