內瑞維歐
K 號：K223169 · 2023-02-06
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器材摘要
Nerivio is the device name listed in this FDA 510(k) record. The listed applicant is Theranica Bioelectronics , Ltd.. It received FDA 510(k) clearance on 2023-02-06 under 510(k) number K223169. The device is classified under product code QGT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Nerivio?
Nerivio is a medical device that received FDA 510(k) clearance on 2023-02-06. The listed applicant is Theranica Bioelectronics , Ltd.. The 510(k) number is K223169.
When did Nerivio receive FDA 510(k) clearance?
Nerivio received FDA 510(k) clearance on 2023-02-06, under 510(k) number K223169.
Who is the listed applicant for Nerivio?
The FDA 510(k) record lists Theranica Bioelectronics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nerivio?
The FDA product code for Nerivio is QGT.
相關臨床試驗
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其他以 Theranica Bioelectronics , Ltd. 為申請人之記錄
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：QGT）
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。
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