迷你美迪 Go App
K 號：K253512 · 2026-01-08
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器材摘要
MiniMed Go App is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 2026-01-08 under 510(k) number K253512. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MiniMed Go App?
MiniMed Go App is a medical device that received FDA 510(k) clearance on 2026-01-08. The listed applicant is Medtronic Minimed. The 510(k) number is K253512.
When did MiniMed Go App receive FDA 510(k) clearance?
MiniMed Go App received FDA 510(k) clearance on 2026-01-08, under 510(k) number K253512.
Who is the listed applicant for MiniMed Go App?
The FDA 510(k) record lists Medtronic Minimed as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MiniMed Go App?
The FDA product code for MiniMed Go App is NDC.
相關臨床試驗
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其他以 Medtronic Minimed 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。
相關器械（代碼：NDC）
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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