D·Kutting™ LL 頸外週圍評分擴張針管
K 號：K242254 · 2025-04-21
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器材摘要
常見問題
What is the D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter?
D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2025-04-21. The listed applicant is Dk Medical Technology Co., Ltd.. The 510(k) number is K242254.
When did D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter receive FDA 510(k) clearance?
D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter received FDA 510(k) clearance on 2025-04-21, under 510(k) number K242254.
Who is the listed applicant for D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter?
The FDA 510(k) record lists Dk Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter?
The FDA product code for D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter is PNO.
相關臨床試驗
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其他以 Dk Medical Technology Co., Ltd. 為申請人之記錄
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：PNO）
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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