單獨式Dex Fascile連續周邊神經阻斷針筒及針頭組合
K 號:K151072 · 2016-01-22
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器材摘要
常見問題
What is the Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit?
Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit is a medical device that received FDA 510(k) clearance on 2016-01-22. The listed applicant is Solo-Dex, Inc.. The 510(k) number is K151072.
When did Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit receive FDA 510(k) clearance?
Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit received FDA 510(k) clearance on 2016-01-22, under 510(k) number K151072.
Who is the listed applicant for Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit?
The FDA 510(k) record lists Solo-Dex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit?
The FDA product code for Solo-Dex Fascile Continuous Peripheral Nerve Block Catheter and Needle Kit is BSP.
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相關器械(代碼:BSP)
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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