Everyway OTC电肌肉刺激（EMS），型号EV-805
K号: K162744 · 2017-08-03
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决定日期2017-08-03
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
Everyway OTC EMS, Model EV-805 is the device name listed in this FDA 510(k) record. The listed applicant is Everyway Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2017-08-03 under 510(k) number K162744. 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 Everyway OTC EMS, Model EV-805?
Everyway OTC EMS, Model EV-805 is a medical device that received FDA 510(k) clearance on 2017-08-03. The listed applicant is Everyway Medical Instrument Co., Ltd.. The 510(k) number is K162744.
When did Everyway OTC EMS, Model EV-805 receive FDA 510(k) clearance?
Everyway OTC EMS, Model EV-805 received FDA 510(k) clearance on 2017-08-03, under 510(k) number K162744.
Who is the listed applicant for Everyway OTC EMS, Model EV-805?
The FDA 510(k) record lists Everyway Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Everyway OTC EMS, Model EV-805?
The FDA product code for Everyway OTC EMS, Model EV-805 is NGX.
相关临床试验
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列明Everyway Medical Instrument Co., Ltd.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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