FDA 510(k)

Voyant® 開放融合設備 (EB240/Open Fusion)

K 號：K252740 · 2025-11-04

決定日期2025-11-04

產品代碼GEI

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Voyant® Open Fusion Device (EB240/Open Fusion) is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2025-11-04 under 510(k) number K252740. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Voyant® Open Fusion Device (EB240/Open Fusion)?

Voyant® Open Fusion Device (EB240/Open Fusion) is a medical device that received FDA 510(k) clearance on 2025-11-04. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K252740.

When did Voyant® Open Fusion Device (EB240/Open Fusion) receive FDA 510(k) clearance?

Voyant® Open Fusion Device (EB240/Open Fusion) received FDA 510(k) clearance on 2025-11-04, under 510(k) number K252740.

Who is the listed applicant for Voyant® Open Fusion Device (EB240/Open Fusion)?

The FDA 510(k) record lists Applied Medical Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Voyant® Open Fusion Device (EB240/Open Fusion)?

The FDA product code for Voyant® Open Fusion Device (EB240/Open Fusion) is GEI.

其他以 Applied Medical Resources Corp. 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。

K252442Kii結構氣球進入系統 K243152GelPOINT V-Path 經陰道進入平台含後腹膜進入裝置 K201212Voyant開放融合裝置 K200598Voyant 馬里蘭融合設備 K193292Voyant 5mm 融合設備，Voyant 馬里蘭融合設備 K191294經陰道進入平台

查看所有 11 項裝置 →

相關器械（代碼：GEI）

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。

K254196HARMONIC 1100 剪刀（HAR1120）；HARMONIC 1100 剪刀（HAR1136）Ethicon Endo-Surgery, LLC K261959Neptune® SafeAir® 10呎煙霧排氣鉛筆，方形包覆，70mm刀片，按鈕開關（0703-046-100）；Neptune® SafeAir® 10呎煙霧排氣鉛筆，方形包覆，按鈕開關，大量非無菌（0703-046-102）；Neptune® SafeAir® 10呎煙霧排氣鉛筆，方形包覆，70mm刀片， rocking 開關（0703-047-100）；Neptune® SafeAir® 10呎煙霧排氣鉛筆，方形包覆，rocking 開關，大量非無菌（0703-047-102）Stryker Instruments K261070LigaSure™ RAS 馬里蘭頰部血管黏合器/分離器，納米塗層Covidien, LLC K254185波坦茲·普瑞美Jeisys Medical Incorporated K262364艾利安恩尼格瑪雷射設備Ellian Corp K253859紅色專業版（Scarlet Pro）VIOL Co., Ltd.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。