Annalise Enterprise CTB Triage-OH
K 號：K231094 · 2023-08-15
廣告
器材摘要
Annalise Enterprise CTB Triage-OH is the device name listed in this FDA 510(k) record. The listed applicant is Annalise-Ai Pty , Ltd.. It received FDA 510(k) clearance on 2023-08-15 under 510(k) number K231094. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Annalise Enterprise CTB Triage-OH?
Annalise Enterprise CTB Triage-OH is a medical device that received FDA 510(k) clearance on 2023-08-15. The listed applicant is Annalise-Ai Pty , Ltd.. The 510(k) number is K231094.
When did Annalise Enterprise CTB Triage-OH receive FDA 510(k) clearance?
Annalise Enterprise CTB Triage-OH received FDA 510(k) clearance on 2023-08-15, under 510(k) number K231094.
Who is the listed applicant for Annalise Enterprise CTB Triage-OH?
The FDA 510(k) record lists Annalise-Ai Pty , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Annalise Enterprise CTB Triage-OH?
The FDA product code for Annalise Enterprise CTB Triage-OH is QAS.
相關臨床試驗
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。
其他以 Annalise-Ai Pty , Ltd. 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：QAS）
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。
廣告