经皮神经电刺激与电肌肉刺激器(LY-ET-01, LY-ET-02, LY-ET-04)
K号: K230443 · 2023-05-22
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器械摘要
常见问题
What is the TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04)?
TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04) is a medical device that received FDA 510(k) clearance on 2023-05-22. The listed applicant is Jiangxi Royall Smart Technology Co., Ltd.. The 510(k) number is K230443.
When did TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04) receive FDA 510(k) clearance?
TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04) received FDA 510(k) clearance on 2023-05-22, under 510(k) number K230443.
Who is the listed applicant for TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04)?
The FDA 510(k) record lists Jiangxi Royall Smart Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04)?
The FDA product code for TENS & EMS Device (LY-ET-01, LY-ET-02, LY-ET-04) is NUH.
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:NUH)
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。
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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