迪米RRT系統
K 號：K193005 · 2020-08-28
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器材摘要
DIMI RRT System is the device name listed in this FDA 510(k) record. The listed applicant is Dialco Medical, Inc.. It received FDA 510(k) clearance on 2020-08-28 under 510(k) number K193005. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DIMI RRT System?
DIMI RRT System is a medical device that received FDA 510(k) clearance on 2020-08-28. The listed applicant is Dialco Medical, Inc.. The 510(k) number is K193005.
When did DIMI RRT System receive FDA 510(k) clearance?
DIMI RRT System received FDA 510(k) clearance on 2020-08-28, under 510(k) number K193005.
Who is the listed applicant for DIMI RRT System?
The FDA 510(k) record lists Dialco Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIMI RRT System?
The FDA product code for DIMI RRT System is KDI.
相關臨床試驗
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相關器械（代碼：KDI）
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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