Vivally系统可穿戴，非侵入式神经调节系统和移动应用程序
K号: K220454 · 2023-04-03
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器械摘要
常见问题
What is the Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application?
Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application is a medical device that received FDA 510(k) clearance on 2023-04-03. The listed applicant is Avation Medical, Inc.. The 510(k) number is K220454.
When did Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application receive FDA 510(k) clearance?
Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application received FDA 510(k) clearance on 2023-04-03, under 510(k) number K220454.
Who is the listed applicant for Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application?
The FDA 510(k) record lists Avation Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application?
The FDA product code for Vivally System Wearable, Non-Invasive Neuromodulation System and Mobile Application is NAM.
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：NAM）
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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