Avantik VTM
K 號：K233449 · 2024-07-15
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決定日期2024-07-15
產品代碼JSM
諮詢委員會MI
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決定相當於
器材摘要
Avantik VTM is the device name listed in this FDA 510(k) record. The listed applicant is Hanchang Medic Co., Ltd. (Han Chang Medic). It received FDA 510(k) clearance on 2024-07-15 under 510(k) number K233449. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Avantik VTM?
Avantik VTM is a medical device that received FDA 510(k) clearance on 2024-07-15. The listed applicant is Hanchang Medic Co., Ltd. (Han Chang Medic). The 510(k) number is K233449.
When did Avantik VTM receive FDA 510(k) clearance?
Avantik VTM received FDA 510(k) clearance on 2024-07-15, under 510(k) number K233449.
Who is the listed applicant for Avantik VTM?
The FDA 510(k) record lists Hanchang Medic Co., Ltd. (Han Chang Medic) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avantik VTM?
The FDA product code for Avantik VTM is JSM.
相關臨床試驗
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相關器械（代碼：JSM）
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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