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FDA 510(k)

808nm 半導體激光脫毛機

K 號：K252048 · 2026-02-03

申請人Xi'An Taibo Electronic Technology Co., Ltd.
決定日期2026-02-03
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

808nm semiconductor laser hair removal machine is the device name listed in this FDA 510(k) record. The listed applicant is Xi'An Taibo Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-03 under 510(k) number K252048. 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 808nm semiconductor laser hair removal machine?

808nm semiconductor laser hair removal machine is a medical device that received FDA 510(k) clearance on 2026-02-03. The listed applicant is Xi'An Taibo Electronic Technology Co., Ltd.. The 510(k) number is K252048.

When did 808nm semiconductor laser hair removal machine receive FDA 510(k) clearance?

808nm semiconductor laser hair removal machine received FDA 510(k) clearance on 2026-02-03, under 510(k) number K252048.

Who is the listed applicant for 808nm semiconductor laser hair removal machine?

The FDA 510(k) record lists Xi'An Taibo Electronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 808nm semiconductor laser hair removal machine?

The FDA product code for 808nm semiconductor laser hair removal machine is GEX. This falls under the Gastroenterology category.

相關臨床試驗

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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。

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