馬厄斯PG II 尖銳物品容器
K 號：K170513 · 2017-11-01
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決定日期2017-11-01
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
MAUSER PG II Sharps Container is the device name listed in this FDA 510(k) record. The listed applicant is Mauzer USA, LLC. It received FDA 510(k) clearance on 2017-11-01 under 510(k) number K170513. 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 MAUSER PG II Sharps Container?
MAUSER PG II Sharps Container is a medical device that received FDA 510(k) clearance on 2017-11-01. The listed applicant is Mauzer USA, LLC. The 510(k) number is K170513.
When did MAUSER PG II Sharps Container receive FDA 510(k) clearance?
MAUSER PG II Sharps Container received FDA 510(k) clearance on 2017-11-01, under 510(k) number K170513.
Who is the listed applicant for MAUSER PG II Sharps Container?
The FDA 510(k) record lists Mauzer USA, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAUSER PG II Sharps Container?
The FDA product code for MAUSER PG II Sharps Container 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
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