靜脈夾子，動脈夾子
K 號：K161315 · 2016-08-18
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器材摘要
Vein Clamps, Artery Clamps is the device name listed in this FDA 510(k) record. The listed applicant is Aros Surgical Instruments Corporation. It received FDA 510(k) clearance on 2016-08-18 under 510(k) number K161315. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vein Clamps, Artery Clamps?
Vein Clamps, Artery Clamps is a medical device that received FDA 510(k) clearance on 2016-08-18. The listed applicant is Aros Surgical Instruments Corporation. The 510(k) number is K161315.
When did Vein Clamps, Artery Clamps receive FDA 510(k) clearance?
Vein Clamps, Artery Clamps received FDA 510(k) clearance on 2016-08-18, under 510(k) number K161315.
Who is the listed applicant for Vein Clamps, Artery Clamps?
The FDA 510(k) record lists Aros Surgical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vein Clamps, Artery Clamps?
The FDA product code for Vein Clamps, Artery Clamps is DXC.
相關臨床試驗
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相關器械（代碼：DXC）
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。
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