Alma LipoFlow系统
K号: K171242 · 2017-07-14
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器械摘要
Alma LipoFlow System is the device name listed in this FDA 510(k) record. The listed applicant is Alma Lasers, Inc.. It received FDA 510(k) clearance on 2017-07-14 under 510(k) number K171242. 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 Alma LipoFlow System?
Alma LipoFlow System is a medical device that received FDA 510(k) clearance on 2017-07-14. The listed applicant is Alma Lasers, Inc.. The 510(k) number is K171242.
When did Alma LipoFlow System receive FDA 510(k) clearance?
Alma LipoFlow System received FDA 510(k) clearance on 2017-07-14, under 510(k) number K171242.
Who is the listed applicant for Alma LipoFlow System?
The FDA 510(k) record lists Alma Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Alma LipoFlow System?
The FDA product code for Alma LipoFlow System is MUU.
相关临床试验
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列明Alma Lasers, Inc.为申报人的其他记录
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
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