藍多普血管專家
K 號：K260700 · 2026-07-08
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器材摘要
BlueDop Vascular Expert is the device name listed in this FDA 510(k) record. The listed applicant is BlueDop Medical, Ltd.. It received FDA 510(k) clearance on 2026-07-08 under 510(k) number K260700. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BlueDop Vascular Expert?
BlueDop Vascular Expert is a medical device that received FDA 510(k) clearance on 2026-07-08. The listed applicant is BlueDop Medical, Ltd.. The 510(k) number is K260700.
When did BlueDop Vascular Expert receive FDA 510(k) clearance?
BlueDop Vascular Expert received FDA 510(k) clearance on 2026-07-08, under 510(k) number K260700.
Who is the listed applicant for BlueDop Vascular Expert?
The FDA 510(k) record lists BlueDop Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BlueDop Vascular Expert?
The FDA product code for BlueDop Vascular Expert is DPW.
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：DPW）
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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