DenQ Sub SLA 嵌入系統
K 號：K240977 · 2024-09-13
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器材摘要
DenQ Sub SLA Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Denq. It received FDA 510(k) clearance on 2024-09-13 under 510(k) number K240977. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DenQ Sub SLA Implant System?
DenQ Sub SLA Implant System is a medical device that received FDA 510(k) clearance on 2024-09-13. The listed applicant is Denq. The 510(k) number is K240977.
When did DenQ Sub SLA Implant System receive FDA 510(k) clearance?
DenQ Sub SLA Implant System received FDA 510(k) clearance on 2024-09-13, under 510(k) number K240977.
Who is the listed applicant for DenQ Sub SLA Implant System?
The FDA 510(k) record lists Denq as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DenQ Sub SLA Implant System?
The FDA product code for DenQ Sub SLA Implant System is DZE.
相關臨床試驗
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相關器械（代碼：DZE）
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。
官方來源
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