XO Score LP 皮膚穿剌經皮腔內血管成形術評分導管，XO Score LP 導管
K 號：K221986 · 2022-10-18
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器材摘要
常見問題
What is the XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter?
XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter is a medical device that received FDA 510(k) clearance on 2022-10-18. The listed applicant is Transit Scientific, LLC. The 510(k) number is K221986.
When did XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter receive FDA 510(k) clearance?
XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter received FDA 510(k) clearance on 2022-10-18, under 510(k) number K221986.
Who is the listed applicant for XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter?
The FDA 510(k) record lists Transit Scientific, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter?
The FDA product code for XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter is PNO.
相關臨床試驗
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其他以 Transit Scientific, LLC 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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