精密TC2、精密TC3、精密TC4、SEG 100、SEG 150、SEG200
K 號:K223784 · 2023-04-18
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器材摘要
常見問題
What is the Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200?
Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200 is a medical device that received FDA 510(k) clearance on 2023-04-18. The listed applicant is Deltronix Equipamentos Ltda. The 510(k) number is K223784.
When did Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200 receive FDA 510(k) clearance?
Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200 received FDA 510(k) clearance on 2023-04-18, under 510(k) number K223784.
Who is the listed applicant for Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200?
The FDA 510(k) record lists Deltronix Equipamentos Ltda as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200?
The FDA product code for Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200 is GEI.
相關臨床試驗
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相關器械(代碼:GEI)
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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