Orbit 子视网膜輸送系統
K 號：K182274 · 2018-11-20
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決定日期2018-11-20
產品代碼FMF
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Unknown
器材摘要
Orbit Subretinal Delivery System is the device name listed in this FDA 510(k) record. The listed applicant is Orbit Biomedical, Inc.. It received FDA 510(k) clearance on 2018-11-20 under 510(k) number K182274. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.
常見問題
What is the Orbit Subretinal Delivery System?
Orbit Subretinal Delivery System is a medical device that received FDA 510(k) clearance on 2018-11-20. The listed applicant is Orbit Biomedical, Inc.. The 510(k) number is K182274.
When did Orbit Subretinal Delivery System receive FDA 510(k) clearance?
Orbit Subretinal Delivery System received FDA 510(k) clearance on 2018-11-20, under 510(k) number K182274.
Who is the listed applicant for Orbit Subretinal Delivery System?
The FDA 510(k) record lists Orbit Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Orbit Subretinal Delivery System?
The FDA product code for Orbit Subretinal Delivery System is FMF.
相關臨床試驗
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相關器械（代碼：FMF）
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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