NeuroTrac® MyoPlus Pro (MYO120U)
K号: K243079 · 2025-06-26
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决定日期2025-06-26
产品代码KPI
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同
器械摘要
NeuroTrac® MyoPlus Pro (MYO120U) is the device name listed in this FDA 510(k) record. The listed applicant is Verity Medical , Ltd.. It received FDA 510(k) clearance on 2025-06-26 under 510(k) number K243079. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NeuroTrac® MyoPlus Pro (MYO120U)?
NeuroTrac® MyoPlus Pro (MYO120U) is a medical device that received FDA 510(k) clearance on 2025-06-26. The listed applicant is Verity Medical , Ltd.. The 510(k) number is K243079.
When did NeuroTrac® MyoPlus Pro (MYO120U) receive FDA 510(k) clearance?
NeuroTrac® MyoPlus Pro (MYO120U) received FDA 510(k) clearance on 2025-06-26, under 510(k) number K243079.
Who is the listed applicant for NeuroTrac® MyoPlus Pro (MYO120U)?
The FDA 510(k) record lists Verity Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NeuroTrac® MyoPlus Pro (MYO120U)?
The FDA product code for NeuroTrac® MyoPlus Pro (MYO120U) is KPI.
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：KPI）
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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