Shoocin 引導套件
K 號：K172099 · 2017-10-05
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器材摘要
Shoocin Introducer Kit is the device name listed in this FDA 510(k) record. The listed applicant is Lepu Medical Technology (Beijing) Co., Ltd.. It received FDA 510(k) clearance on 2017-10-05 under 510(k) number K172099. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Shoocin Introducer Kit?
Shoocin Introducer Kit is a medical device that received FDA 510(k) clearance on 2017-10-05. The listed applicant is Lepu Medical Technology (Beijing) Co., Ltd.. The 510(k) number is K172099.
When did Shoocin Introducer Kit receive FDA 510(k) clearance?
Shoocin Introducer Kit received FDA 510(k) clearance on 2017-10-05, under 510(k) number K172099.
Who is the listed applicant for Shoocin Introducer Kit?
The FDA 510(k) record lists Lepu Medical Technology (Beijing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Shoocin Introducer Kit?
The FDA product code for Shoocin Introducer Kit is DYB.
相關臨床試驗
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其他以 Lepu Medical Technology (Beijing) 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：DYB）
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。
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官方來源
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