真空泵（型號：AD-VPUM-500）
K 號：K260194 · 2026-04-28
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決定日期2026-04-28
產品代碼MQG
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
Vacuum Pump (Model: AD-VPUM-500) is the device name listed in this FDA 510(k) record. The listed applicant is Sheng Sheng Yi (Beijing) Technology Company Limited. It received FDA 510(k) clearance on 2026-04-28 under 510(k) number K260194. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vacuum Pump (Model: AD-VPUM-500)?
Vacuum Pump (Model: AD-VPUM-500) is a medical device that received FDA 510(k) clearance on 2026-04-28. The listed applicant is Sheng Sheng Yi (Beijing) Technology Company Limited. The 510(k) number is K260194.
When did Vacuum Pump (Model: AD-VPUM-500) receive FDA 510(k) clearance?
Vacuum Pump (Model: AD-VPUM-500) received FDA 510(k) clearance on 2026-04-28, under 510(k) number K260194.
Who is the listed applicant for Vacuum Pump (Model: AD-VPUM-500)?
The FDA 510(k) record lists Sheng Sheng Yi (Beijing) Technology Company Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vacuum Pump (Model: AD-VPUM-500)?
The FDA product code for Vacuum Pump (Model: AD-VPUM-500) is MQG.
相關臨床試驗
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相關器械（代碼：MQG）
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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