Pivot 系統消毒盒
K 號：K181845 · 2019-11-25
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決定日期2019-11-25
產品代碼KCT
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
Pivot System Sterilization case is the device name listed in this FDA 510(k) record. The listed applicant is Rp Medical, Inc.. It received FDA 510(k) clearance on 2019-11-25 under 510(k) number K181845. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Pivot System Sterilization case?
Pivot System Sterilization case is a medical device that received FDA 510(k) clearance on 2019-11-25. The listed applicant is Rp Medical, Inc.. The 510(k) number is K181845.
When did Pivot System Sterilization case receive FDA 510(k) clearance?
Pivot System Sterilization case received FDA 510(k) clearance on 2019-11-25, under 510(k) number K181845.
Who is the listed applicant for Pivot System Sterilization case?
The FDA 510(k) record lists Rp Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pivot System Sterilization case?
The FDA product code for Pivot System Sterilization case is KCT.
相關臨床試驗
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相關器械（代碼：KCT）
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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