SMARxT 管道及接頭
K 號：K233702 · 2024-08-08
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器材摘要
SMARxT Tubing and Connectors is the device name listed in this FDA 510(k) record. The listed applicant is LivaNova USA, Inc.. It received FDA 510(k) clearance on 2024-08-08 under 510(k) number K233702. The device is classified under product code DWE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SMARxT Tubing and Connectors?
SMARxT Tubing and Connectors is a medical device that received FDA 510(k) clearance on 2024-08-08. The listed applicant is LivaNova USA, Inc.. The 510(k) number is K233702.
When did SMARxT Tubing and Connectors receive FDA 510(k) clearance?
SMARxT Tubing and Connectors received FDA 510(k) clearance on 2024-08-08, under 510(k) number K233702.
Who is the listed applicant for SMARxT Tubing and Connectors?
The FDA 510(k) record lists LivaNova USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SMARxT Tubing and Connectors?
The FDA product code for SMARxT Tubing and Connectors is DWE.
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其他以 LivaNova USA, Inc. 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。
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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