征服水蒸氣消融設備
K 號：K252388 · 2025-11-26
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器材摘要
Vanquish Water Vapor Ablation Device is the device name listed in this FDA 510(k) record. The listed applicant is Francis Medical, Inc.. It received FDA 510(k) clearance on 2025-11-26 under 510(k) number K252388. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vanquish Water Vapor Ablation Device?
Vanquish Water Vapor Ablation Device is a medical device that received FDA 510(k) clearance on 2025-11-26. The listed applicant is Francis Medical, Inc.. The 510(k) number is K252388.
When did Vanquish Water Vapor Ablation Device receive FDA 510(k) clearance?
Vanquish Water Vapor Ablation Device received FDA 510(k) clearance on 2025-11-26, under 510(k) number K252388.
Who is the listed applicant for Vanquish Water Vapor Ablation Device?
The FDA 510(k) record lists Francis Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vanquish Water Vapor Ablation Device?
The FDA product code for Vanquish Water Vapor Ablation Device is KNS.
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相關器械（代碼：KNS）
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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