维泽恩DR + 无线
K号: K160810 · 2016-05-20
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器械摘要
ViZion DR + Wireless is the device name listed in this FDA 510(k) record. The listed applicant is Viztek, LLC. It received FDA 510(k) clearance on 2016-05-20 under 510(k) number K160810. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ViZion DR + Wireless?
ViZion DR + Wireless is a medical device that received FDA 510(k) clearance on 2016-05-20. The listed applicant is Viztek, LLC. The 510(k) number is K160810.
When did ViZion DR + Wireless receive FDA 510(k) clearance?
ViZion DR + Wireless received FDA 510(k) clearance on 2016-05-20, under 510(k) number K160810.
Who is the listed applicant for ViZion DR + Wireless?
The FDA 510(k) record lists Viztek, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ViZion DR + Wireless?
The FDA product code for ViZion DR + Wireless is MQB.
相关临床试验
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相关器械（代码：MQB）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
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