V20、V20a、AVSM3 SNF
K 號：K200434 · 2020-10-09
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器材摘要
V20, V20a, AVSM3 SNF is the device name listed in this FDA 510(k) record. The listed applicant is Mediana Co., Ltd.. It received FDA 510(k) clearance on 2020-10-09 under 510(k) number K200434. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the V20, V20a, AVSM3 SNF?
V20, V20a, AVSM3 SNF is a medical device that received FDA 510(k) clearance on 2020-10-09. The listed applicant is Mediana Co., Ltd.. The 510(k) number is K200434.
When did V20, V20a, AVSM3 SNF receive FDA 510(k) clearance?
V20, V20a, AVSM3 SNF received FDA 510(k) clearance on 2020-10-09, under 510(k) number K200434.
Who is the listed applicant for V20, V20a, AVSM3 SNF?
The FDA 510(k) record lists Mediana Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for V20, V20a, AVSM3 SNF?
The FDA product code for V20, V20a, AVSM3 SNF is DXN.
其他以 Mediana Co., Ltd. 為申請人之記錄
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相關器械（代碼：DXN）
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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