Argos
K 號：K181372 · 2018-12-13
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器材摘要
Argos is the device name listed in this FDA 510(k) record. The listed applicant is Retia Medical, LLC. It received FDA 510(k) clearance on 2018-12-13 under 510(k) number K181372. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Argos?
Argos is a medical device that received FDA 510(k) clearance on 2018-12-13. The listed applicant is Retia Medical, LLC. The 510(k) number is K181372.
When did Argos receive FDA 510(k) clearance?
Argos received FDA 510(k) clearance on 2018-12-13, under 510(k) number K181372.
Who is the listed applicant for Argos?
The FDA 510(k) record lists Retia Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Argos?
The FDA product code for Argos is DXG.
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相關器械（代碼：DXG）
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
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