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FDA 510(k)

F1 母船無線傳感器，用於胎兒超聲波和宮縮計監測

K 號：K171865 · 2017-08-24

申請人Farus, LLC
決定日期2017-08-24
產品代碼HGM
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

F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring is the device name listed in this FDA 510(k) record. The listed applicant is Farus, LLC. It received FDA 510(k) clearance on 2017-08-24 under 510(k) number K171865. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring?

F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring is a medical device that received FDA 510(k) clearance on 2017-08-24. The listed applicant is Farus, LLC. The 510(k) number is K171865.

When did F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring receive FDA 510(k) clearance?

F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring received FDA 510(k) clearance on 2017-08-24, under 510(k) number K171865.

Who is the listed applicant for F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring?

The FDA 510(k) record lists Farus, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring?

The FDA product code for F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring is HGM.

相關臨床試驗

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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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。

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官方來源

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