Utepreva 子宮內膜採樣器 (UP01)
K 號：K240595 · 2024-08-14
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決定日期2024-08-14
產品代碼HFE
諮詢委員會OB設備之醫療設備規範文本翻譯如下：
關於OB設備的醫療設備規範文件：
此設備已通過FDA認證，並獲得510(k)許可證。該設備的PMA申請已提交，並在NCT登錄編號為[編號]的研究中進行測試。相關文獻的PMID編號為[編號]。請參考以下識別碼和網址：
識別碼：[識別碼]
網址：[網址]
政策：醫療規範-v1
決定相當於
器材摘要
Utepreva Endometrial Sampler (UP01) is the device name listed in this FDA 510(k) record. The listed applicant is Utepreva, LLC. It received FDA 510(k) clearance on 2024-08-14 under 510(k) number K240595. The device is classified under product code HFE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Utepreva Endometrial Sampler (UP01)?
Utepreva Endometrial Sampler (UP01) is a medical device that received FDA 510(k) clearance on 2024-08-14. The listed applicant is Utepreva, LLC. The 510(k) number is K240595.
When did Utepreva Endometrial Sampler (UP01) receive FDA 510(k) clearance?
Utepreva Endometrial Sampler (UP01) received FDA 510(k) clearance on 2024-08-14, under 510(k) number K240595.
Who is the listed applicant for Utepreva Endometrial Sampler (UP01)?
The FDA 510(k) record lists Utepreva, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Utepreva Endometrial Sampler (UP01)?
The FDA product code for Utepreva Endometrial Sampler (UP01) is HFE.
相關臨床試驗
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相關器械（代碼：HFE）
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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