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FDA 510(k)

IPL治療設備（MDSQMC-01）

K 號：K243123 · 2025-07-03

申請人Medusa (Guangxi)Medical Devices Co., Ltd.
決定日期2025-07-03
產品代碼ONF
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

IPL Treatment Device (MDSQMC-01) is the device name listed in this FDA 510(k) record. The listed applicant is Medusa (Guangxi)Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2025-07-03 under 510(k) number K243123. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the IPL Treatment Device (MDSQMC-01)?

IPL Treatment Device (MDSQMC-01) is a medical device that received FDA 510(k) clearance on 2025-07-03. The listed applicant is Medusa (Guangxi)Medical Devices Co., Ltd.. The 510(k) number is K243123.

When did IPL Treatment Device (MDSQMC-01) receive FDA 510(k) clearance?

IPL Treatment Device (MDSQMC-01) received FDA 510(k) clearance on 2025-07-03, under 510(k) number K243123.

Who is the listed applicant for IPL Treatment Device (MDSQMC-01)?

The FDA 510(k) record lists Medusa (Guangxi)Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPL Treatment Device (MDSQMC-01)?

The FDA product code for IPL Treatment Device (MDSQMC-01) is ONF.

相關臨床試驗

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：ONF）

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。

K261204強烈脈衝光療法設備Sanhe LEFIS Electronics Co., Ltd.K251545強烈脈衝光療法設備（MMABM-1）Micowey Medical Equipment (Guangxi) Co., Ltd.K231952醫療設備名稱：MEDILIGHTMedicreations, LLCK250281DEKA 草莓El.En S.P.A.K242440強烈脈衝光治療系統（LK-PT）Nanjing Bestview Laser S&T Co., Ltd.K240314MULA (K2-A1)Guangzhou Ciellulu Photoelectric Technology Co., Ltd.

官方來源

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