FDA 510(k)

醫用二極雷射系統

K 號：K230047 · 2024-03-04

決定日期2024-03-04

產品代碼NVK

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

Medical Diode Laser Systems is the device name listed in this FDA 510(k) record. The listed applicant is Gigaalaser Company , Ltd.. It received FDA 510(k) clearance on 2024-03-04 under 510(k) number K230047. The device is classified under product code NVK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Medical Diode Laser Systems?

Medical Diode Laser Systems is a medical device that received FDA 510(k) clearance on 2024-03-04. The listed applicant is Gigaalaser Company , Ltd.. The 510(k) number is K230047.

When did Medical Diode Laser Systems receive FDA 510(k) clearance?

Medical Diode Laser Systems received FDA 510(k) clearance on 2024-03-04, under 510(k) number K230047.

Who is the listed applicant for Medical Diode Laser Systems?

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

What is the FDA product code for Medical Diode Laser Systems?

The FDA product code for Medical Diode Laser Systems is NVK.

其他以 Gigaalaser Company , Ltd. 為申請人之記錄

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相關器械（代碼：NVK）

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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