TUBETECH IV 輸注設備組
K 號：K162951 · 2017-07-28
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決定日期2017-07-28
產品代碼FPA
諮詢委員會醫療設備規範文本翻譯如下：
HO
注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於
器材摘要
TUBETECH IV Administration Set is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Medical Products, Inc.. It received FDA 510(k) clearance on 2017-07-28 under 510(k) number K162951. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TUBETECH IV Administration Set?
TUBETECH IV Administration Set is a medical device that received FDA 510(k) clearance on 2017-07-28. The listed applicant is Douglas Medical Products, Inc.. The 510(k) number is K162951.
When did TUBETECH IV Administration Set receive FDA 510(k) clearance?
TUBETECH IV Administration Set received FDA 510(k) clearance on 2017-07-28, under 510(k) number K162951.
Who is the listed applicant for TUBETECH IV Administration Set?
The FDA 510(k) record lists Douglas Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBETECH IV Administration Set?
The FDA product code for TUBETECH IV Administration Set is FPA.
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。
相關器械（代碼：FPA）
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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