FDA 510(k)

Duetto Suprema；Domino Suprema；Suprema VT；Suprema VT+；Suprema 4V

K 號：K223404 · 2023-01-20

決定日期2023-01-20

產品代碼GEX

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

Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V is the device name listed in this FDA 510(k) record. The listed applicant is Quanta System Spa. It received FDA 510(k) clearance on 2023-01-20 under 510(k) number K223404. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V?

Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V is a medical device that received FDA 510(k) clearance on 2023-01-20. The listed applicant is Quanta System Spa. The 510(k) number is K223404.

When did Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V receive FDA 510(k) clearance?

Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V received FDA 510(k) clearance on 2023-01-20, under 510(k) number K223404.

Who is the listed applicant for Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V?

The FDA 510(k) record lists Quanta System Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V?

The FDA product code for Duetto Suprema; Domino Suprema; Suprema VT; Suprema VT+; Suprema 4V is GEX. This falls under the Gastroenterology category.

其他以 Quanta System Spa 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。

K240983Discovery Pico；Discovery Pico Plus；Discovery Pico 皮膚 K243588單次使用二氧化碳激光纖維（HAF005001）K241092Youlaser PRIME；Youlaser PRIME CO2；Youlaser PRIME MT K242251立石60；立石100；立石150 K232236回聲 K220426纖維塵 PRO

查看所有 34 項裝置 →

相關器械（代碼：GEX）

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。

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro 系列Fotona D.O.O.K241973SmartIPL_NI 系統Lumenis Be, Ltd.K261047牙科二極雷射設備（雷射筆）Guilin Kevin Peter Technology Co., Ltd.K261817二極雷射治療系統（PZ-BDT67-01，PZ-BDT67-02）Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED治療設備（QLXY-01）Beijing Nubway S&T 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。