漢姆頓-G5
K 號：K180295 · 2019-07-30
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器材摘要
Hamilton-G5 is the device name listed in this FDA 510(k) record. The listed applicant is Hamiton Medical AG. It received FDA 510(k) clearance on 2019-07-30 under 510(k) number K180295. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Hamilton-G5?
Hamilton-G5 is a medical device that received FDA 510(k) clearance on 2019-07-30. The listed applicant is Hamiton Medical AG. The 510(k) number is K180295.
When did Hamilton-G5 receive FDA 510(k) clearance?
Hamilton-G5 received FDA 510(k) clearance on 2019-07-30, under 510(k) number K180295.
Who is the listed applicant for Hamilton-G5?
The FDA 510(k) record lists Hamiton Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hamilton-G5?
The FDA product code for Hamilton-G5 is CBK.
相關臨床試驗
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相關器械（代碼：CBK）
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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