DORA 血液透析管路套件
K 號:K161582 · 2017-06-16
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器材摘要
常見問題
What is the DORA Tubing Sets for Hemodialysis?
DORA Tubing Sets for Hemodialysis is a medical device that received FDA 510(k) clearance on 2017-06-16. The listed applicant is Bain Medical Equipment (Guangzhou) Co., Ltd.. The 510(k) number is K161582.
When did DORA Tubing Sets for Hemodialysis receive FDA 510(k) clearance?
DORA Tubing Sets for Hemodialysis received FDA 510(k) clearance on 2017-06-16, under 510(k) number K161582.
Who is the listed applicant for DORA Tubing Sets for Hemodialysis?
The FDA 510(k) record lists Bain Medical Equipment (Guangzhou) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DORA Tubing Sets for Hemodialysis?
The FDA product code for DORA Tubing Sets for Hemodialysis is FJK.
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其他以 Bain Medical Equipment (Guangzhou) 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:FJK)
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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