尼達M&T安全箱
K 號：K211464 · 2021-09-14
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決定日期2021-09-14
產品代碼MMK
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
Nitta M&T Safety Box is the device name listed in this FDA 510(k) record. The listed applicant is Nitta M&T (Thailand) Co., Ltd.. It received FDA 510(k) clearance on 2021-09-14 under 510(k) number K211464. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Nitta M&T Safety Box?
Nitta M&T Safety Box is a medical device that received FDA 510(k) clearance on 2021-09-14. The listed applicant is Nitta M&T (Thailand) Co., Ltd.. The 510(k) number is K211464.
When did Nitta M&T Safety Box receive FDA 510(k) clearance?
Nitta M&T Safety Box received FDA 510(k) clearance on 2021-09-14, under 510(k) number K211464.
Who is the listed applicant for Nitta M&T Safety Box?
The FDA 510(k) record lists Nitta M&T (Thailand) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nitta M&T Safety Box?
The FDA product code for Nitta M&T Safety Box is MMK.
相關臨床試驗
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相關器械（代碼：MMK）
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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