Sonicaid Team3 分娩前期,Sonicaid Team3 分娩期
K 號:K200975 · 2020-06-24
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器材摘要
常見問題
What is the Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum?
Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum is a medical device that received FDA 510(k) clearance on 2020-06-24. The listed applicant is Huntleigh Healthcare Limited. The 510(k) number is K200975.
When did Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum receive FDA 510(k) clearance?
Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum received FDA 510(k) clearance on 2020-06-24, under 510(k) number K200975.
Who is the listed applicant for Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum?
The FDA 510(k) record lists Huntleigh Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum?
The FDA product code for Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum is HGM.
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其他以 Huntleigh Healthcare Limited 為申請人之記錄
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。
相關器械(代碼:HGM)
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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