威爾斯針
K 號：K172120 · 2017-09-14
廣告
器材摘要
Veress Needle is the device name listed in this FDA 510(k) record. The listed applicant is Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. It received FDA 510(k) clearance on 2017-09-14 under 510(k) number K172120. The device is classified under product code FHO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Veress Needle?
Veress Needle is a medical device that received FDA 510(k) clearance on 2017-09-14. The listed applicant is Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. The 510(k) number is K172120.
When did Veress Needle receive FDA 510(k) clearance?
Veress Needle received FDA 510(k) clearance on 2017-09-14, under 510(k) number K172120.
Who is the listed applicant for Veress Needle?
The FDA 510(k) record lists Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Veress Needle?
The FDA product code for Veress Needle is FHO.
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 Wickimed (Huizhou) Medical Equipment Manufacturing 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。
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