脂質蛋白，低密度，移除
PMA 核准號：P940016 · 2019-06-07
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器材摘要
Lipoprotein, low density, removal is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun Avitum AG. It received FDA 510(k) clearance on 2019-06-07. The device is classified under product code MMY. It was reviewed by the GU advisory panel.
常見問題
What is the Lipoprotein, low density, removal?
Lipoprotein, low density, removal is a medical device that received FDA 510(k) clearance on 2019-06-07. The listed applicant is B. Braun Avitum AG.
When did Lipoprotein, low density, removal receive FDA 510(k) clearance?
The clearance date for Lipoprotein, low density, removal can be found in the official FDA records.
Who is the listed applicant for Lipoprotein, low density, removal?
The FDA 510(k) record lists B. Braun Avitum AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lipoprotein, low density, removal?
The FDA product code for Lipoprotein, low density, removal is MMY.
相關臨床試驗
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官方來源
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