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FDA 510(k)

達芬奇 E-200 電外科電流發生器

K 號:K223039 · 2022-11-28

決定日期2022-11-28
產品代碼GEI
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

da Vinci E-200 Electrosurgical Generator is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical. It received FDA 510(k) clearance on 2022-11-28 under 510(k) number K223039. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the da Vinci E-200 Electrosurgical Generator?

da Vinci E-200 Electrosurgical Generator is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Intuitive Surgical. The 510(k) number is K223039.

When did da Vinci E-200 Electrosurgical Generator receive FDA 510(k) clearance?

da Vinci E-200 Electrosurgical Generator received FDA 510(k) clearance on 2022-11-28, under 510(k) number K223039.

Who is the listed applicant for da Vinci E-200 Electrosurgical Generator?

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

What is the FDA product code for da Vinci E-200 Electrosurgical Generator?

The FDA product code for da Vinci E-200 Electrosurgical Generator is GEI.

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其他以 Intuitive Surgical 為申請人之記錄

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相關器械(代碼:GEI)

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官方來源

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