VIDAvision
K 號：K200990 · 2020-08-07
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器材摘要
VIDAvision is the device name listed in this FDA 510(k) record. The listed applicant is Vida Diagnostics, Inc.. It received FDA 510(k) clearance on 2020-08-07 under 510(k) number K200990. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VIDAvision?
VIDAvision is a medical device that received FDA 510(k) clearance on 2020-08-07. The listed applicant is Vida Diagnostics, Inc.. The 510(k) number is K200990.
When did VIDAvision receive FDA 510(k) clearance?
VIDAvision received FDA 510(k) clearance on 2020-08-07, under 510(k) number K200990.
Who is the listed applicant for VIDAvision?
The FDA 510(k) record lists Vida Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIDAvision?
The FDA product code for VIDAvision is JAK.
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相關器械（代碼：JAK）
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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