VIA 17 微导管
K 號：K162565 · 2017-02-18
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器材摘要
VIA 17 Microcatheter is the device name listed in this FDA 510(k) record. The listed applicant is Sequent Medical, Inc.. It received FDA 510(k) clearance on 2017-02-18 under 510(k) number K162565. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VIA 17 Microcatheter?
VIA 17 Microcatheter is a medical device that received FDA 510(k) clearance on 2017-02-18. The listed applicant is Sequent Medical, Inc.. The 510(k) number is K162565.
When did VIA 17 Microcatheter receive FDA 510(k) clearance?
VIA 17 Microcatheter received FDA 510(k) clearance on 2017-02-18, under 510(k) number K162565.
Who is the listed applicant for VIA 17 Microcatheter?
The FDA 510(k) record lists Sequent Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIA 17 Microcatheter?
The FDA product code for VIA 17 Microcatheter is DQY.
相關臨床試驗
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相關器械（代碼：DQY）
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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