FDA 510(k)

矽鎵纖維雷射機器（FiberLAZE+、FiberLAZE）

K 號：K242987 · 2024-12-17

申請人Allengers Global Healthcare Private Limited

決定日期2024-12-17

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

Thulium Fiber Laser (FiberLAZE+, FiberLAZE) is the device name listed in this FDA 510(k) record. The listed applicant is Allengers Global Healthcare Private Limited. It received FDA 510(k) clearance on 2024-12-17 under 510(k) number K242987. 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 Thulium Fiber Laser (FiberLAZE+, FiberLAZE)?

Thulium Fiber Laser (FiberLAZE+, FiberLAZE) is a medical device that received FDA 510(k) clearance on 2024-12-17. The listed applicant is Allengers Global Healthcare Private Limited. The 510(k) number is K242987.

When did Thulium Fiber Laser (FiberLAZE+, FiberLAZE) receive FDA 510(k) clearance?

Thulium Fiber Laser (FiberLAZE+, FiberLAZE) received FDA 510(k) clearance on 2024-12-17, under 510(k) number K242987.

Who is the listed applicant for Thulium Fiber Laser (FiberLAZE+, FiberLAZE)?

The FDA 510(k) record lists Allengers Global Healthcare Private Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Thulium Fiber Laser (FiberLAZE+, FiberLAZE)?

The FDA product code for Thulium Fiber Laser (FiberLAZE+, FiberLAZE) is GEX. This falls under the Gastroenterology category.

其他以 Allengers Global Healthcare Private Limited 為申請人之記錄

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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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