FDA 510(k)

Scorpion 鋒針門腔靜脈進入組合，Scorpion 鋒針門腔靜脈進入組合

K 號：K202141 · 2021-01-15

決定日期2021-01-15

產品代碼DYB

諮詢委員會履歷

決定相當於

器材摘要

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2021-01-15 under 510(k) number K202141. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is a medical device that received FDA 510(k) clearance on 2021-01-15. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K202141.

When did Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set receive FDA 510(k) clearance?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set received FDA 510(k) clearance on 2021-01-15, under 510(k) number K202141.

Who is the listed applicant for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

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

What is the FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

The FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is DYB.

其他以 Argon Medical Devices, Inc. 為申請人之記錄

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相關器械（代碼：DYB）

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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