Moxxly流量收集系统
K号: K170722 · 2017-08-28
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申请人Moxxly, Inc.
决定日期2017-08-28
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
Moxxly Flow Collection System is the device name listed in this FDA 510(k) record. The listed applicant is Moxxly, Inc.. It received FDA 510(k) clearance on 2017-08-28 under 510(k) number K170722. 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 Moxxly Flow Collection System?
Moxxly Flow Collection System is a medical device that received FDA 510(k) clearance on 2017-08-28. The listed applicant is Moxxly, Inc.. The 510(k) number is K170722.
When did Moxxly Flow Collection System receive FDA 510(k) clearance?
Moxxly Flow Collection System received FDA 510(k) clearance on 2017-08-28, under 510(k) number K170722.
Who is the listed applicant for Moxxly Flow Collection System?
The FDA 510(k) record lists Moxxly, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Moxxly Flow Collection System?
The FDA product code for Moxxly Flow Collection System is HGX.
相关临床试验
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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
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