維薩留斯
K 號：K152933 · 2016-03-23
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器材摘要
Vesalius is the device name listed in this FDA 510(k) record. The listed applicant is Telea Electronic Engineering Srl. It received FDA 510(k) clearance on 2016-03-23 under 510(k) number K152933. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vesalius?
Vesalius is a medical device that received FDA 510(k) clearance on 2016-03-23. The listed applicant is Telea Electronic Engineering Srl. The 510(k) number is K152933.
When did Vesalius receive FDA 510(k) clearance?
Vesalius received FDA 510(k) clearance on 2016-03-23, under 510(k) number K152933.
Who is the listed applicant for Vesalius?
The FDA 510(k) record lists Telea Electronic Engineering Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vesalius?
The FDA product code for Vesalius is GEI.
相關臨床試驗
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相關器械（代碼：GEI）
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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官方來源
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