Freemie 独立性，Freemie 自由
K号: K172772 · 2017-10-13
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申请人Dao Health
决定日期2017-10-13
产品代码HGX
咨询委员会OB
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决定实质等同
器械摘要
Freemie Independence, Freemie Liberty is the device name listed in this FDA 510(k) record. The listed applicant is Dao Health. It received FDA 510(k) clearance on 2017-10-13 under 510(k) number K172772. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Freemie Independence, Freemie Liberty?
Freemie Independence, Freemie Liberty is a medical device that received FDA 510(k) clearance on 2017-10-13. The listed applicant is Dao Health. The 510(k) number is K172772.
When did Freemie Independence, Freemie Liberty receive FDA 510(k) clearance?
Freemie Independence, Freemie Liberty received FDA 510(k) clearance on 2017-10-13, under 510(k) number K172772.
Who is the listed applicant for Freemie Independence, Freemie Liberty?
The FDA 510(k) record lists Dao Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Freemie Independence, Freemie Liberty?
The FDA product code for Freemie Independence, Freemie Liberty is HGX.
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：HGX）
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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