RelieforMe TENS/EMS 裝置 型號 UPK-GE01
K 號：K192733 · 2019-12-23
廣告
器材摘要
RelieforMe TENS/EMS Device Model UPK-GE01 is the device name listed in this FDA 510(k) record. The listed applicant is Umeheal , Ltd.. It received FDA 510(k) clearance on 2019-12-23 under 510(k) number K192733. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the RelieforMe TENS/EMS Device Model UPK-GE01?
RelieforMe TENS/EMS Device Model UPK-GE01 is a medical device that received FDA 510(k) clearance on 2019-12-23. The listed applicant is Umeheal , Ltd.. The 510(k) number is K192733.
When did RelieforMe TENS/EMS Device Model UPK-GE01 receive FDA 510(k) clearance?
RelieforMe TENS/EMS Device Model UPK-GE01 received FDA 510(k) clearance on 2019-12-23, under 510(k) number K192733.
Who is the listed applicant for RelieforMe TENS/EMS Device Model UPK-GE01?
The FDA 510(k) record lists Umeheal , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RelieforMe TENS/EMS Device Model UPK-GE01?
The FDA product code for RelieforMe TENS/EMS Device Model UPK-GE01 is IPF.
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：IPF）
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