ARISTE AB 網格
K 號：K211132 · 2022-03-18
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器材摘要
ARISTE AB Mesh is the device name listed in this FDA 510(k) record. The listed applicant is Ariste Medical, LLC. It received FDA 510(k) clearance on 2022-03-18 under 510(k) number K211132. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ARISTE AB Mesh?
ARISTE AB Mesh is a medical device that received FDA 510(k) clearance on 2022-03-18. The listed applicant is Ariste Medical, LLC. The 510(k) number is K211132.
When did ARISTE AB Mesh receive FDA 510(k) clearance?
ARISTE AB Mesh received FDA 510(k) clearance on 2022-03-18, under 510(k) number K211132.
Who is the listed applicant for ARISTE AB Mesh?
The FDA 510(k) record lists Ariste Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARISTE AB Mesh?
The FDA product code for ARISTE AB Mesh is FTL.
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。
相關器械（代碼：FTL）
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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