S698 Symbioz 流量計
K 號：K153367 · 2016-06-17
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決定日期2016-06-17
產品代碼HIF
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
S698 Symbioz flow is the device name listed in this FDA 510(k) record. The listed applicant is Sopro - Acteon Group. It received FDA 510(k) clearance on 2016-06-17 under 510(k) number K153367. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the S698 Symbioz flow?
S698 Symbioz flow is a medical device that received FDA 510(k) clearance on 2016-06-17. The listed applicant is Sopro - Acteon Group. The 510(k) number is K153367.
When did S698 Symbioz flow receive FDA 510(k) clearance?
S698 Symbioz flow received FDA 510(k) clearance on 2016-06-17, under 510(k) number K153367.
Who is the listed applicant for S698 Symbioz flow?
The FDA 510(k) record lists Sopro - Acteon Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S698 Symbioz flow?
The FDA product code for S698 Symbioz flow is HIF.
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相關器械（代碼：HIF）
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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