電外科發生器及附件
K 號：K201224 · 2020-09-18
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器材摘要
Electrosurgical Generator and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Medrange. It received FDA 510(k) clearance on 2020-09-18 under 510(k) number K201224. 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 and Accessories?
Electrosurgical Generator and Accessories is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is Medrange. The 510(k) number is K201224.
When did Electrosurgical Generator and Accessories receive FDA 510(k) clearance?
Electrosurgical Generator and Accessories received FDA 510(k) clearance on 2020-09-18, under 510(k) number K201224.
Who is the listed applicant for Electrosurgical Generator and Accessories?
The FDA 510(k) record lists Medrange as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electrosurgical Generator and Accessories?
The FDA product code for Electrosurgical Generator and Accessories is GEI.
相關臨床試驗
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。
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。
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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