FDA 510(k)

Aventus 引入鞘

K 號：K260091 · 2026-04-13

決定日期2026-04-13

產品代碼DYB

諮詢委員會履歷

決定相當於

器材摘要

Aventus Introducer Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Inquis Medical. It received FDA 510(k) clearance on 2026-04-13 under 510(k) number K260091. 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 Aventus Introducer Sheath?

Aventus Introducer Sheath is a medical device that received FDA 510(k) clearance on 2026-04-13. The listed applicant is Inquis Medical. The 510(k) number is K260091.

When did Aventus Introducer Sheath receive FDA 510(k) clearance?

Aventus Introducer Sheath received FDA 510(k) clearance on 2026-04-13, under 510(k) number K260091.

Who is the listed applicant for Aventus Introducer Sheath?

FDA 510(k) 記錄將 Inquis Medical 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Aventus Introducer Sheath?

The FDA product code for Aventus Introducer Sheath is DYB.

其他以 Inquis Medical 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。

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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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官方來源

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