AeviceMD
K 號：K223382 · 2023-07-07
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器材摘要
AeviceMD is the device name listed in this FDA 510(k) record. The listed applicant is Aevice Health Pte. , Ltd.. It received FDA 510(k) clearance on 2023-07-07 under 510(k) number K223382. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AeviceMD?
AeviceMD is a medical device that received FDA 510(k) clearance on 2023-07-07. The listed applicant is Aevice Health Pte. , Ltd.. The 510(k) number is K223382.
When did AeviceMD receive FDA 510(k) clearance?
AeviceMD received FDA 510(k) clearance on 2023-07-07, under 510(k) number K223382.
Who is the listed applicant for AeviceMD?
The FDA 510(k) record lists Aevice Health Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AeviceMD?
The FDA product code for AeviceMD is DSH.
相關臨床試驗
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其他以 Aevice Health Pte. , 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：DSH）
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
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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