腸胃邊界識別器（GIBI HD）
K 號：K221898 · 2022-07-28
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器材摘要
常見問題
What is the Gastrointestinal Boundary Identifier (GIBI HD)?
Gastrointestinal Boundary Identifier (GIBI HD) is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Reshape Lifesciences. The 510(k) number is K221898.
When did Gastrointestinal Boundary Identifier (GIBI HD) receive FDA 510(k) clearance?
Gastrointestinal Boundary Identifier (GIBI HD) received FDA 510(k) clearance on 2022-07-28, under 510(k) number K221898.
Who is the listed applicant for Gastrointestinal Boundary Identifier (GIBI HD)?
The FDA 510(k) record lists Reshape Lifesciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gastrointestinal Boundary Identifier (GIBI HD)?
The FDA product code for Gastrointestinal Boundary Identifier (GIBI HD) is KNT.
相關臨床試驗
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其他以 Reshape Lifesciences 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：KNT）
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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