可重用單極活動電纜
K 號：K192518 · 2019-10-25
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器材摘要
Reusable Monopolar Active Cord is the device name listed in this FDA 510(k) record. The listed applicant is Us Endoscopy. It received FDA 510(k) clearance on 2019-10-25 under 510(k) number K192518. 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 Reusable Monopolar Active Cord?
Reusable Monopolar Active Cord is a medical device that received FDA 510(k) clearance on 2019-10-25. The listed applicant is Us Endoscopy. The 510(k) number is K192518.
When did Reusable Monopolar Active Cord receive FDA 510(k) clearance?
Reusable Monopolar Active Cord received FDA 510(k) clearance on 2019-10-25, under 510(k) number K192518.
Who is the listed applicant for Reusable Monopolar Active Cord?
The FDA 510(k) record lists Us Endoscopy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reusable Monopolar Active Cord?
The FDA product code for Reusable Monopolar Active Cord is GEI.
相關臨床試驗
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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。
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官方來源
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