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FDA 510(k)

Trio-CT® 三腔管心臟內科導管配曲式延伸管

K 號:K232945 · 2023-11-16

決定日期2023-11-16
產品代碼NIE
諮詢委員會GU
決定Unknown

器材摘要

Trio-CT­® Triple Lumen Catheter w/ Curved Extensions is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc. (dba MedComp). It received FDA 510(k) clearance on 2023-11-16 under 510(k) number K232945. The device is classified under product code NIE. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常見問題

What is the Trio-CT­® Triple Lumen Catheter w/ Curved Extensions?

Trio-CT­® Triple Lumen Catheter w/ Curved Extensions is a medical device that received FDA 510(k) clearance on 2023-11-16. The listed applicant is Medical Components, Inc. (dba MedComp). The 510(k) number is K232945.

When did Trio-CT­® Triple Lumen Catheter w/ Curved Extensions receive FDA 510(k) clearance?

Trio-CT­® Triple Lumen Catheter w/ Curved Extensions received FDA 510(k) clearance on 2023-11-16, under 510(k) number K232945.

Who is the listed applicant for Trio-CT­® Triple Lumen Catheter w/ Curved Extensions?

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

What is the FDA product code for Trio-CT­® Triple Lumen Catheter w/ Curved Extensions?

The FDA product code for Trio-CT­® Triple Lumen Catheter w/ Curved Extensions is NIE.

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其他以 Medical Components, Inc. (dba MedComp) 為申請人之記錄

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相關器械(代碼:NIE)

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