精瘦UP超級
K 號：K151722 · 2016-03-18
廣告
器材摘要
Slim UP ULTRA is the device name listed in this FDA 510(k) record. The listed applicant is Aime Medical, Inc.. It received FDA 510(k) clearance on 2016-03-18 under 510(k) number K151722. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Slim UP ULTRA?
Slim UP ULTRA is a medical device that received FDA 510(k) clearance on 2016-03-18. The listed applicant is Aime Medical, Inc.. The 510(k) number is K151722.
When did Slim UP ULTRA receive FDA 510(k) clearance?
Slim UP ULTRA received FDA 510(k) clearance on 2016-03-18, under 510(k) number K151722.
Who is the listed applicant for Slim UP ULTRA?
The FDA 510(k) record lists Aime Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Slim UP ULTRA?
The FDA product code for Slim UP ULTRA is NGX.
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：NGX）
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。
K253790高強度聚焦電磁刺激器（FE60）Beijing Winkonlaser Technology LimitedK253926迪阿科爾ShenB Co., Ltd.K253636Zionic Pro Max (電動肌肉刺激器)Termosalud S.L.K253408涼頻Zimmer Medizinsysteme GmbHK252154攜帶式電刺激治療設備（LGT-2320BE、LGT-2320ME 及 LGT-2320SP）Guangzhou Longest Medical Technology Co., Ltd.K253478Motive™ 腰部肌肉刺激器 (OT01-1003)Motive Health, Inc.
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