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FDA 510(k)

電外科發生器 ESG-410,腳踏開關,PK 切割鉗子

K 號:K203277 · 2021-04-28

決定日期2021-04-28
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

Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Winter & Ibe GmbH. It received FDA 510(k) clearance on 2021-04-28 under 510(k) number K203277. 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 Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps?

Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps is a medical device that received FDA 510(k) clearance on 2021-04-28. The listed applicant is Olympus Winter & Ibe GmbH. The 510(k) number is K203277.

When did Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps receive FDA 510(k) clearance?

Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps received FDA 510(k) clearance on 2021-04-28, under 510(k) number K203277.

Who is the listed applicant for Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps?

The FDA 510(k) record lists Olympus Winter & Ibe GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps?

The FDA product code for Electrosurgical Generator ESG-410, Foot Switches, PK Cutting Forceps is GEI.

相關臨床試驗

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其他以 Olympus Winter & Ibe GmbH 為申請人之記錄

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相關器械(代碼:GEI)

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。

官方來源

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