清淨UP 鼻炎痛緩解
K 號：K182025 · 2019-01-02
廣告
器材摘要
ClearUP Sinus Pain Relief is the device name listed in this FDA 510(k) record. The listed applicant is Tivic Health Systems, Inc.. It received FDA 510(k) clearance on 2019-01-02 under 510(k) number K182025. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ClearUP Sinus Pain Relief?
ClearUP Sinus Pain Relief is a medical device that received FDA 510(k) clearance on 2019-01-02. The listed applicant is Tivic Health Systems, Inc.. The 510(k) number is K182025.
When did ClearUP Sinus Pain Relief receive FDA 510(k) clearance?
ClearUP Sinus Pain Relief received FDA 510(k) clearance on 2019-01-02, under 510(k) number K182025.
Who is the listed applicant for ClearUP Sinus Pain Relief?
The FDA 510(k) record lists Tivic Health Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ClearUP Sinus Pain Relief?
The FDA product code for ClearUP Sinus Pain Relief is GZJ.
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：GZJ）
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