系統83旋轉內視鏡清潔/消毒器
K 號：K241168 · 2024-12-19
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器材摘要
System 83 Revolve Endoscope Washer/Disinfector is the device name listed in this FDA 510(k) record. The listed applicant is Wassenburg Medical, Inc.. It received FDA 510(k) clearance on 2024-12-19 under 510(k) number K241168. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the System 83 Revolve Endoscope Washer/Disinfector?
System 83 Revolve Endoscope Washer/Disinfector is a medical device that received FDA 510(k) clearance on 2024-12-19. The listed applicant is Wassenburg Medical, Inc.. The 510(k) number is K241168.
When did System 83 Revolve Endoscope Washer/Disinfector receive FDA 510(k) clearance?
System 83 Revolve Endoscope Washer/Disinfector received FDA 510(k) clearance on 2024-12-19, under 510(k) number K241168.
Who is the listed applicant for System 83 Revolve Endoscope Washer/Disinfector?
The FDA 510(k) record lists Wassenburg Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for System 83 Revolve Endoscope Washer/Disinfector?
The FDA product code for System 83 Revolve Endoscope Washer/Disinfector is FEB.
相關臨床試驗
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相關器械（代碼：FEB）
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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