EndoCure 模型 EUR078A
K 號：K161147 · 2016-06-07
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器材摘要
EndoCure Model EUR078A is the device name listed in this FDA 510(k) record. The listed applicant is Endocure Technologies, Inc.. It received FDA 510(k) clearance on 2016-06-07 under 510(k) number K161147. The device is classified under product code FBN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the EndoCure Model EUR078A?
EndoCure Model EUR078A is a medical device that received FDA 510(k) clearance on 2016-06-07. The listed applicant is Endocure Technologies, Inc.. The 510(k) number is K161147.
When did EndoCure Model EUR078A receive FDA 510(k) clearance?
EndoCure Model EUR078A received FDA 510(k) clearance on 2016-06-07, under 510(k) number K161147.
Who is the listed applicant for EndoCure Model EUR078A?
The FDA 510(k) record lists Endocure Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EndoCure Model EUR078A?
The FDA product code for EndoCure Model EUR078A is FBN.
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相關器械（代碼：FBN）
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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