達芬奇手持式攝影機
K 號：K241913 · 2024-08-28
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器材摘要
da Vinci Handheld Camera is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical Operations, Inc.. It received FDA 510(k) clearance on 2024-08-28 under 510(k) number K241913. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the da Vinci Handheld Camera?
da Vinci Handheld Camera is a medical device that received FDA 510(k) clearance on 2024-08-28. The listed applicant is Intuitive Surgical Operations, Inc.. The 510(k) number is K241913.
When did da Vinci Handheld Camera receive FDA 510(k) clearance?
da Vinci Handheld Camera received FDA 510(k) clearance on 2024-08-28, under 510(k) number K241913.
Who is the listed applicant for da Vinci Handheld Camera?
The FDA 510(k) record lists Intuitive Surgical Operations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for da Vinci Handheld Camera?
The FDA product code for da Vinci Handheld Camera is GCJ.
相關臨床試驗
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相關器械（代碼：GCJ）
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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