維克多 VT-300
K 號：K231575 · 2024-02-08
廣告
器材摘要
Vecttor VT-300 is the device name listed in this FDA 510(k) record. The listed applicant is Artaflex, Inc.. It received FDA 510(k) clearance on 2024-02-08 under 510(k) number K231575. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vecttor VT-300?
Vecttor VT-300 is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is Artaflex, Inc.. The 510(k) number is K231575.
When did Vecttor VT-300 receive FDA 510(k) clearance?
Vecttor VT-300 received FDA 510(k) clearance on 2024-02-08, under 510(k) number K231575.
Who is the listed applicant for Vecttor VT-300?
The FDA 510(k) record lists Artaflex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vecttor VT-300?
The FDA product code for Vecttor VT-300 is LIH.
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：LIH）
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