永昇黏膜提升劑
K 號：K202376 · 2020-09-30
廣告
器材摘要
EverLift Submucosal Lifting Agent is the device name listed in this FDA 510(k) record. The listed applicant is Gi Supply, Inc.. It received FDA 510(k) clearance on 2020-09-30 under 510(k) number K202376. The device is classified under product code PLL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the EverLift Submucosal Lifting Agent?
EverLift Submucosal Lifting Agent is a medical device that received FDA 510(k) clearance on 2020-09-30. The listed applicant is Gi Supply, Inc.. The 510(k) number is K202376.
When did EverLift Submucosal Lifting Agent receive FDA 510(k) clearance?
EverLift Submucosal Lifting Agent received FDA 510(k) clearance on 2020-09-30, under 510(k) number K202376.
Who is the listed applicant for EverLift Submucosal Lifting Agent?
The FDA 510(k) record lists Gi Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EverLift Submucosal Lifting Agent?
The FDA product code for EverLift Submucosal Lifting Agent is PLL.
相關臨床試驗
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。
其他以 Gi Supply, Inc. 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：PLL）
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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