視覺身體
K 號：K222386 · 2023-02-24
廣告
器材摘要
Visionbody is the device name listed in this FDA 510(k) record. The listed applicant is Vb Technologies AG. It received FDA 510(k) clearance on 2023-02-24 under 510(k) number K222386. 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 Visionbody?
Visionbody is a medical device that received FDA 510(k) clearance on 2023-02-24. The listed applicant is Vb Technologies AG. The 510(k) number is K222386.
When did Visionbody receive FDA 510(k) clearance?
Visionbody received FDA 510(k) clearance on 2023-02-24, under 510(k) number K222386.
Who is the listed applicant for Visionbody?
The FDA 510(k) record lists Vb Technologies AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Visionbody?
The FDA product code for Visionbody 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