Compex Sport Elite
K号: K170918 · 2017-06-20
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申请人Djo, LLC
决定日期2017-06-20
产品代码NGX
咨询委员会PM
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决定实质等同
器械摘要
Compex Sport Elite is the device name listed in this FDA 510(k) record. The listed applicant is Djo, LLC. It received FDA 510(k) clearance on 2017-06-20 under 510(k) number K170918. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Compex Sport Elite?
Compex Sport Elite is a medical device that received FDA 510(k) clearance on 2017-06-20. The listed applicant is Djo, LLC. The 510(k) number is K170918.
When did Compex Sport Elite receive FDA 510(k) clearance?
Compex Sport Elite received FDA 510(k) clearance on 2017-06-20, under 510(k) number K170918.
Who is the listed applicant for Compex Sport Elite?
The FDA 510(k) record lists Djo, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Compex Sport Elite?
The FDA product code for Compex Sport Elite is NGX.
相关临床试验
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列明Djo, LLC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：NGX）
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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