藥物釋放周邊經皮腔內血管成形術導管
PMA 核准號：P210039 · 2023-08-16
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器材摘要
Drug-Eluting Peripheral Transluminal Angioplasty Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Trireme Medical, LLC. It received FDA 510(k) clearance on 2023-08-16. The device is classified under product code ONU. It was reviewed by the CV advisory panel.
常見問題
What is the Drug-Eluting Peripheral Transluminal Angioplasty Catheter?
Drug-Eluting Peripheral Transluminal Angioplasty Catheter is a medical device that received FDA 510(k) clearance on 2023-08-16. The listed applicant is Trireme Medical, LLC.
When did Drug-Eluting Peripheral Transluminal Angioplasty Catheter receive FDA 510(k) clearance?
The clearance date for Drug-Eluting Peripheral Transluminal Angioplasty Catheter can be found in the official FDA records.
誰是藥物釋放性周邊經皮腔內血管成形術導管的登記申請人？
The FDA 510(k) record lists Trireme Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？藥物釋放性周邊經皮腔內血管成形術導管？
FDA產品代碼，針對藥物釋放性周邊經皮腔內血管成形術導管為ONU。
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。
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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