KTA脂肪治疗套件
K号: K190386 · 2019-10-10
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器械摘要
KTA Adipose Treatment Kit is the device name listed in this FDA 510(k) record. The listed applicant is Stemics S.A.S. It received FDA 510(k) clearance on 2019-10-10 under 510(k) number K190386. 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 KTA Adipose Treatment Kit?
KTA Adipose Treatment Kit is a medical device that received FDA 510(k) clearance on 2019-10-10. The listed applicant is Stemics S.A.S. The 510(k) number is K190386.
When did KTA Adipose Treatment Kit receive FDA 510(k) clearance?
KTA Adipose Treatment Kit received FDA 510(k) clearance on 2019-10-10, under 510(k) number K190386.
Who is the listed applicant for KTA Adipose Treatment Kit?
The FDA 510(k) record lists Stemics S.A.S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KTA Adipose Treatment Kit?
The FDA product code for KTA Adipose Treatment Kit is MUU.
相关临床试验
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。
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
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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