X-View 3D 全景/X-View 2D 全景
K 號：K222666 · 2023-07-10
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器材摘要
X-View 3D Pan/X-View 2D Pan is the device name listed in this FDA 510(k) record. The listed applicant is Trident S.R.L. It received FDA 510(k) clearance on 2023-07-10 under 510(k) number K222666. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the X-View 3D Pan/X-View 2D Pan?
X-View 3D Pan/X-View 2D Pan is a medical device that received FDA 510(k) clearance on 2023-07-10. The listed applicant is Trident S.R.L. The 510(k) number is K222666.
When did X-View 3D Pan/X-View 2D Pan receive FDA 510(k) clearance?
X-View 3D Pan/X-View 2D Pan received FDA 510(k) clearance on 2023-07-10, under 510(k) number K222666.
Who is the listed applicant for X-View 3D Pan/X-View 2D Pan?
The FDA 510(k) record lists Trident S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-View 3D Pan/X-View 2D Pan?
The FDA product code for X-View 3D Pan/X-View 2D Pan is OAS.
其他以 Trident S.R.L 為申請人之記錄
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相關器械（代碼：OAS）
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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