ClariVein IC
K 號：K153502 · 2016-01-06
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器材摘要
ClariVein IC is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Insights, LLC. It received FDA 510(k) clearance on 2016-01-06 under 510(k) number K153502. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ClariVein IC?
ClariVein IC is a medical device that received FDA 510(k) clearance on 2016-01-06. The listed applicant is Vascular Insights, LLC. The 510(k) number is K153502.
When did ClariVein IC receive FDA 510(k) clearance?
ClariVein IC received FDA 510(k) clearance on 2016-01-06, under 510(k) number K153502.
Who is the listed applicant for ClariVein IC?
The FDA 510(k) record lists Vascular Insights, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ClariVein IC?
The FDA product code for ClariVein IC is KRA.
相關臨床試驗
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相關器械（代碼：KRA）
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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