VIDAvision
K号: K200990 · 2020-08-07
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器械摘要
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.
常见问题
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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相关器械（代码：JAK）
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