PerQseal 引導器
K 號：K252309 · 2025-10-23
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器材摘要
PerQseal Introducers is the device name listed in this FDA 510(k) record. The listed applicant is Vivasure Medical Limited. It received FDA 510(k) clearance on 2025-10-23 under 510(k) number K252309. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PerQseal Introducers?
PerQseal Introducers is a medical device that received FDA 510(k) clearance on 2025-10-23. The listed applicant is Vivasure Medical Limited. The 510(k) number is K252309.
When did PerQseal Introducers receive FDA 510(k) clearance?
PerQseal Introducers received FDA 510(k) clearance on 2025-10-23, under 510(k) number K252309.
Who is the listed applicant for PerQseal Introducers?
The FDA 510(k) record lists Vivasure Medical Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PerQseal Introducers?
The FDA product code for PerQseal Introducers is DYB.
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相關器械（代碼：DYB）
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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