Vivally 系統穿戴式，非侵入性神經調節系統及行動應用程序
K 號：K220454 · 2023-04-03
廣告
器材摘要
常見問題
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.
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
相關器械（代碼：NAM）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
廣告