陰道觸覺超音波影像儀
K 號：K231875 · 2024-02-22
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決定日期2024-02-22
產品代碼HIR
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
Vaginal Tactile Ultrasound Imager is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Tactile Imaging, Inc.. It received FDA 510(k) clearance on 2024-02-22 under 510(k) number K231875. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vaginal Tactile Ultrasound Imager?
Vaginal Tactile Ultrasound Imager is a medical device that received FDA 510(k) clearance on 2024-02-22. The listed applicant is Advanced Tactile Imaging, Inc.. The 510(k) number is K231875.
When did Vaginal Tactile Ultrasound Imager receive FDA 510(k) clearance?
Vaginal Tactile Ultrasound Imager received FDA 510(k) clearance on 2024-02-22, under 510(k) number K231875.
Who is the listed applicant for Vaginal Tactile Ultrasound Imager?
The FDA 510(k) record lists Advanced Tactile Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vaginal Tactile Ultrasound Imager?
The FDA product code for Vaginal Tactile Ultrasound Imager is HIR.
相關臨床試驗
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相關器械（代碼：HIR）
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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