Whiterabbit.ai的WRDensity
K号: K202013 · 2020-10-30
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器械摘要
WRDensity by Whiterabbit.ai is the device name listed in this FDA 510(k) record. The listed applicant is Whiterabbit.Ai, Inc.. It received FDA 510(k) clearance on 2020-10-30 under 510(k) number K202013. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the WRDensity by Whiterabbit.ai?
WRDensity by Whiterabbit.ai is a medical device that received FDA 510(k) clearance on 2020-10-30. The listed applicant is Whiterabbit.Ai, Inc.. The 510(k) number is K202013.
When did WRDensity by Whiterabbit.ai receive FDA 510(k) clearance?
WRDensity by Whiterabbit.ai received FDA 510(k) clearance on 2020-10-30, under 510(k) number K202013.
Who is the listed applicant for WRDensity by Whiterabbit.ai?
The FDA 510(k) record lists Whiterabbit.Ai, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WRDensity by Whiterabbit.ai?
The FDA product code for WRDensity by Whiterabbit.ai is QIH.
相关临床试验
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相关器械（代码：QIH）
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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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