FDA 510(k)

對比™ 管針 (VS110-9NB)

K 號：K260149 · 2026-02-17

決定日期2026-02-17

產品代碼QEY

諮詢委員會履歷

決定相當於

器材摘要

Versus™ Catheter (VS110-9NB) is the device name listed in this FDA 510(k) record. The listed applicant is Liquet Medical, Inc.. It received FDA 510(k) clearance on 2026-02-17 under 510(k) number K260149. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Versus™ Catheter (VS110-9NB)?

Versus™ Catheter (VS110-9NB) is a medical device that received FDA 510(k) clearance on 2026-02-17. The listed applicant is Liquet Medical, Inc.. The 510(k) number is K260149.

When did Versus™ Catheter (VS110-9NB) receive FDA 510(k) clearance?

Versus™ Catheter (VS110-9NB) received FDA 510(k) clearance on 2026-02-17, under 510(k) number K260149.

Who is the listed applicant for Versus™ Catheter (VS110-9NB)?

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

What is the FDA product code for Versus™ Catheter (VS110-9NB)?

The FDA product code for Versus™ Catheter (VS110-9NB) is QEY.

其他以 Liquet Medical, Inc. 為申請人之記錄

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。

K241851對比™ 管針 (VS110-8B)

相關器械（代碼：QEY）

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。

K251318變頻調節輸液針管Argon Medical Devices, Inc.K241851對比™ 管針 (VS110-8B)Liquet Medical, Inc.K231653BASHIR™ .035內血管導管，BASHIR™ S-B .035內血管導管Thrombolex, Inc.K222095BASHIR內血管導管參考編號7201，BASHIR S-B內血管導管，參考編號7101Thrombolex, Inc.K220866EKOS+內血管設備Boston Scientific K213422EkoSonic內血管設備，EKOS+內血管設備Boston Scientific Corporation

官方來源

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