ViMove2
K号: K163150 · 2017-07-14
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决定日期2017-07-14
产品代码IKN
咨询委员会PM
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决定实质等同
器械摘要
ViMove2 is the device name listed in this FDA 510(k) record. The listed applicant is Dorsavi, Ltd.. It received FDA 510(k) clearance on 2017-07-14 under 510(k) number K163150. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ViMove2?
ViMove2 is a medical device that received FDA 510(k) clearance on 2017-07-14. The listed applicant is Dorsavi, Ltd.. The 510(k) number is K163150.
When did ViMove2 receive FDA 510(k) clearance?
ViMove2 received FDA 510(k) clearance on 2017-07-14, under 510(k) number K163150.
Who is the listed applicant for ViMove2?
The FDA 510(k) record lists Dorsavi, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ViMove2?
The FDA product code for ViMove2 is IKN.
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相关器械（代码：IKN）
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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