InVera 靜脈輸注設備
K 號：K250794 · 2026-03-12
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器材摘要
InVera Infusion Device is the device name listed in this FDA 510(k) record. The listed applicant is Invera Medical. It received FDA 510(k) clearance on 2026-03-12 under 510(k) number K250794. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the InVera Infusion Device?
InVera Infusion Device is a medical device that received FDA 510(k) clearance on 2026-03-12. The listed applicant is Invera Medical. The 510(k) number is K250794.
When did InVera Infusion Device receive FDA 510(k) clearance?
InVera Infusion Device received FDA 510(k) clearance on 2026-03-12, under 510(k) number K250794.
Who is the listed applicant for InVera Infusion Device?
The FDA 510(k) record lists Invera Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InVera Infusion Device?
The FDA product code for InVera Infusion Device is KRA.
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相關器械（代碼：KRA）
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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