Prismira
K 號：K243729 · 2025-06-13
廣告
決定日期2025-06-13
產品代碼QFT
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
Prismira is the device name listed in this FDA 510(k) record. The listed applicant is Lumos Labs, Inc.. It received FDA 510(k) clearance on 2025-06-13 under 510(k) number K243729. The device is classified under product code QFT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Prismira?
Prismira is a medical device that received FDA 510(k) clearance on 2025-06-13. The listed applicant is Lumos Labs, Inc.. The 510(k) number is K243729.
When did Prismira receive FDA 510(k) clearance?
Prismira received FDA 510(k) clearance on 2025-06-13, under 510(k) number K243729.
Who is the listed applicant for Prismira?
The FDA 510(k) record lists Lumos Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prismira?
The FDA product code for Prismira is QFT.
相關臨床試驗
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相關器械（代碼：QFT）
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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