LipiVage
K号: K172714 · 2017-12-08
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决定日期2017-12-08
产品代码MUU
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
LipiVage is the device name listed in this FDA 510(k) record. The listed applicant is Genesis Biosystems, Inc.. It received FDA 510(k) clearance on 2017-12-08 under 510(k) number K172714. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LipiVage?
LipiVage is a medical device that received FDA 510(k) clearance on 2017-12-08. The listed applicant is Genesis Biosystems, Inc.. The 510(k) number is K172714.
When did LipiVage receive FDA 510(k) clearance?
LipiVage received FDA 510(k) clearance on 2017-12-08, under 510(k) number K172714.
Who is the listed applicant for LipiVage?
The FDA 510(k) record lists Genesis Biosystems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LipiVage?
The FDA product code for LipiVage is MUU.
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相关器械（代码：MUU）
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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