FDA 510(k)

Dermalux 三波長 MD MKII (1000021)；Dermalux 細巧型 MD (1000024)

K 號：K240222 · 2024-06-04

決定日期2024-06-04

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

Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) is the device name listed in this FDA 510(k) record. The listed applicant is Aesthetic Technology, Ltd.. It received FDA 510(k) clearance on 2024-06-04 under 510(k) number K240222. 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 Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)?

Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) is a medical device that received FDA 510(k) clearance on 2024-06-04. The listed applicant is Aesthetic Technology, Ltd.. The 510(k) number is K240222.

When did Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) receive FDA 510(k) clearance?

Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) received FDA 510(k) clearance on 2024-06-04, under 510(k) number K240222.

Who is the listed applicant for Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)?

The FDA 510(k) record lists Aesthetic Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)?

The FDA product code for Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) is GEX. This falls under the Gastroenterology category.

其他以 Aesthetic Technology, Ltd. 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。

K212275皮膚輝光 Flex MDF K202028dermalux Flex MD K200659皮膚輝 Tri-Wave 醫療設備

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。