DENU 輕體(標準，快速)，DENU 重體(標準，快速)，DENU 黏土組合(標準，快速)
K 號：K222741 · 2022-11-07
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器材摘要
常見問題
What is the DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast)?
DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast) is a medical device that received FDA 510(k) clearance on 2022-11-07. The listed applicant is Hdi, Inc.. The 510(k) number is K222741.
When did DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast) receive FDA 510(k) clearance?
DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast) received FDA 510(k) clearance on 2022-11-07, under 510(k) number K222741.
Who is the listed applicant for DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast)?
The FDA 510(k) record lists Hdi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast)?
The FDA product code for DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast) is ELW.
相關臨床試驗
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其他以 Hdi, Inc. 為申請人之記錄
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。
相關器械（代碼：ELW）
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
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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