Vesocclude 聚合物結合夾
K 號：K152082 · 2016-02-26
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器材摘要
Vesocclude Polymer Ligating Clip is the device name listed in this FDA 510(k) record. The listed applicant is Vesocclude Medical, LLC. It received FDA 510(k) clearance on 2016-02-26 under 510(k) number K152082. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vesocclude Polymer Ligating Clip?
Vesocclude Polymer Ligating Clip is a medical device that received FDA 510(k) clearance on 2016-02-26. The listed applicant is Vesocclude Medical, LLC. The 510(k) number is K152082.
When did Vesocclude Polymer Ligating Clip receive FDA 510(k) clearance?
Vesocclude Polymer Ligating Clip received FDA 510(k) clearance on 2016-02-26, under 510(k) number K152082.
Who is the listed applicant for Vesocclude Polymer Ligating Clip?
The FDA 510(k) record lists Vesocclude Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vesocclude Polymer Ligating Clip?
The FDA product code for Vesocclude Polymer Ligating Clip is FZP.
相關臨床試驗
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相關器械（代碼：FZP）
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
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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