Tangent單次使用數位系統：Tangent單次使用數位心导管及Tangent數位控制器
K 號：K251170 · 2025-09-12
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器材摘要
常見問題
What is the Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller?
Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller is a medical device that received FDA 510(k) clearance on 2025-09-12. The listed applicant is Tangent Endoscopy, LLC. The 510(k) number is K251170.
When did Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller receive FDA 510(k) clearance?
Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller received FDA 510(k) clearance on 2025-09-12, under 510(k) number K251170.
Who is the listed applicant for Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller?
The FDA 510(k) record lists Tangent Endoscopy, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller?
The FDA product code for Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller is FBN.
相關臨床試驗
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相關器械（代碼：FBN）
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。
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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