Geomed 頸動脈擴張器
K 號：K183438 · 2019-09-03
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器材摘要
Geomed Vascular Dilators is the device name listed in this FDA 510(k) record. The listed applicant is Geomed Medizin-Technik GmbH & Co.. It received FDA 510(k) clearance on 2019-09-03 under 510(k) number K183438. The device is classified under product code DWP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Geomed Vascular Dilators?
Geomed Vascular Dilators is a medical device that received FDA 510(k) clearance on 2019-09-03. The listed applicant is Geomed Medizin-Technik GmbH & Co.. The 510(k) number is K183438.
When did Geomed Vascular Dilators receive FDA 510(k) clearance?
Geomed Vascular Dilators received FDA 510(k) clearance on 2019-09-03, under 510(k) number K183438.
Who is the listed applicant for Geomed Vascular Dilators?
The FDA 510(k) record lists Geomed Medizin-Technik GmbH & Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Geomed Vascular Dilators?
The FDA product code for Geomed Vascular Dilators is DWP.
相關臨床試驗
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相關器械（代碼：DWP）
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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