括約肌斷刀 / 短線兼容型,无菌括約肌斷刀
K 號:K210934 · 2021-12-01
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器材摘要
常見問題
What is the Sphincterotome / short-wire compatible, Sterile Sphincterotome?
Sphincterotome / short-wire compatible, Sterile Sphincterotome is a medical device that received FDA 510(k) clearance on 2021-12-01. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K210934.
When did Sphincterotome / short-wire compatible, Sterile Sphincterotome receive FDA 510(k) clearance?
Sphincterotome / short-wire compatible, Sterile Sphincterotome received FDA 510(k) clearance on 2021-12-01, under 510(k) number K210934.
Who is the listed applicant for Sphincterotome / short-wire compatible, Sterile Sphincterotome?
The FDA 510(k) record lists Micro-Tech (Nanjing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sphincterotome / short-wire compatible, Sterile Sphincterotome?
The FDA product code for Sphincterotome / short-wire compatible, Sterile Sphincterotome is KNS.
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 Micro-Tech (Nanjing) 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:KNS)
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。
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