FDA 510(k)

Symetrex 長期血液透析針管

K 號：K171618 · 2017-11-16

申請人Medcomp (Dba Medical Components, Inc.)

決定日期2017-11-16

產品代碼MSD

諮詢委員會GU

決定Unknown

器材摘要

Symetrex Long Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp (Dba Medical Components, Inc.). It received FDA 510(k) clearance on 2017-11-16 under 510(k) number K171618. 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 Symetrex Long Term Hemodialysis Catheter?

Symetrex Long Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is Medcomp (Dba Medical Components, Inc.). The 510(k) number is K171618.

When did Symetrex Long Term Hemodialysis Catheter receive FDA 510(k) clearance?

Symetrex Long Term Hemodialysis Catheter received FDA 510(k) clearance on 2017-11-16, under 510(k) number K171618.

Who is the listed applicant for Symetrex Long Term Hemodialysis Catheter?

The FDA 510(k) record lists Medcomp (Dba Medical Components, Inc.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Symetrex Long Term Hemodialysis Catheter?

The FDA product code for Symetrex Long Term Hemodialysis Catheter is MSD.

其他以 Medcomp (Dba Medical Components, 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。

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官方來源

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