FDA 510(k)

GlidePath 13F 長期血液透析針管

K 號：K211410 · 2021-06-04

決定日期2021-06-04

產品代碼MSD

諮詢委員會GU

決定Unknown

器材摘要

GlidePath 13F Long-Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2021-06-04 under 510(k) number K211410. 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 GlidePath 13F Long-Term Hemodialysis Catheter?

GlidePath 13F Long-Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2021-06-04. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K211410.

When did GlidePath 13F Long-Term Hemodialysis Catheter receive FDA 510(k) clearance?

GlidePath 13F Long-Term Hemodialysis Catheter received FDA 510(k) clearance on 2021-06-04, under 510(k) number K211410.

Who is the listed applicant for GlidePath 13F Long-Term Hemodialysis Catheter?

FDA 510(k) 記錄將 Bard Peripheral Vascular, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for GlidePath 13F Long-Term Hemodialysis Catheter?

The FDA product code for GlidePath 13F Long-Term Hemodialysis Catheter is MSD.

其他以 Bard Peripheral Vascular, Inc. 為申請人之記錄

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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 Corporation K210461終端蓋Medical Components Inc (Medcomp)K203575GlidePath 長期血液透析導管C.R. Bard, Inc.K203767純淨長期血液透析針管C B Bard, 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

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