Talent-Pro 電磁刺激器
K 號：K202031 · 2021-05-06
廣告
器材摘要
Talent-Pro Electromagnetic Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Remed Co., Ltd.. It received FDA 510(k) clearance on 2021-05-06 under 510(k) number K202031. 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 Talent-Pro Electromagnetic Stimulator?
Talent-Pro Electromagnetic Stimulator is a medical device that received FDA 510(k) clearance on 2021-05-06. The listed applicant is Remed Co., Ltd.. The 510(k) number is K202031.
When did Talent-Pro Electromagnetic Stimulator receive FDA 510(k) clearance?
Talent-Pro Electromagnetic Stimulator received FDA 510(k) clearance on 2021-05-06, under 510(k) number K202031.
Who is the listed applicant for Talent-Pro Electromagnetic Stimulator?
The FDA 510(k) record lists Remed Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Talent-Pro Electromagnetic Stimulator?
The FDA product code for Talent-Pro Electromagnetic Stimulator 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。
其他以 Remed Co., 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：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