FDA 510(k)

IPG醫療系列：鐵礦紡織激光器、外科紡織和配件

K 號：K232568 · 2024-03-21

決定日期2024-03-21

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

IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Ipg Medical Corporation. It received FDA 510(k) clearance on 2024-03-21 under 510(k) number K232568. 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 IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories?

IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories is a medical device that received FDA 510(k) clearance on 2024-03-21. The listed applicant is Ipg Medical Corporation. The 510(k) number is K232568.

When did IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories receive FDA 510(k) clearance?

IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories received FDA 510(k) clearance on 2024-03-21, under 510(k) number K232568.

Who is the listed applicant for IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories?

The FDA 510(k) record lists Ipg Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories?

The FDA product code for IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories is GEX. This falls under the Gastroenterology category.

其他以 Ipg Medical Corporation 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。

K251100IPGTFL-02

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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官方來源

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