純淨長期血液透析針管
K 號：K203767 · 2021-04-02
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器材摘要
Pristine Long-Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C B Bard, Inc.. It received FDA 510(k) clearance on 2021-04-02 under 510(k) number K203767. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常見問題
What is the Pristine Long-Term Hemodialysis Catheter?
Pristine Long-Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is C B Bard, Inc.. The 510(k) number is K203767.
When did Pristine Long-Term Hemodialysis Catheter receive FDA 510(k) clearance?
Pristine Long-Term Hemodialysis Catheter received FDA 510(k) clearance on 2021-04-02, under 510(k) number K203767.
Who is the listed applicant for Pristine Long-Term Hemodialysis Catheter?
The FDA 510(k) record lists C B Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pristine Long-Term Hemodialysis Catheter?
The FDA product code for Pristine Long-Term Hemodialysis Catheter is MSD.
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：MSD）
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。
K241581血液透析針管Haolang Medical USA CorporationK210461終端蓋Medical Components Inc (Medcomp)K203575GlidePath 長期血液透析導管C.R. Bard, Inc.K211410GlidePath 13F 長期血液透析針管Bard Peripheral Vascular, Inc.K202150GlidePath 7.5F 長期透析針管C.R. Bard, Inc.K202176Symetrex LTHD 穿刺管，附側孔的 Symetrex LTHD 穿刺管Medical Components, Inc. (dba MedComp)
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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