VACUETTE® 快速保護完整（加強版）
K 號：K233979 · 2024-07-19
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器材摘要
VACUETTE® QUICKSHIELD Complete (Plus) is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Bio-One North America, Inc.. It received FDA 510(k) clearance on 2024-07-19 under 510(k) number K233979. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VACUETTE® QUICKSHIELD Complete (Plus)?
VACUETTE® QUICKSHIELD Complete (Plus) is a medical device that received FDA 510(k) clearance on 2024-07-19. The listed applicant is Greiner Bio-One North America, Inc.. The 510(k) number is K233979.
When did VACUETTE® QUICKSHIELD Complete (Plus) receive FDA 510(k) clearance?
VACUETTE® QUICKSHIELD Complete (Plus) received FDA 510(k) clearance on 2024-07-19, under 510(k) number K233979.
Who is the listed applicant for VACUETTE® QUICKSHIELD Complete (Plus)?
The FDA 510(k) record lists Greiner Bio-One North America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VACUETTE® QUICKSHIELD Complete (Plus)?
The FDA product code for VACUETTE® QUICKSHIELD Complete (Plus) is JKA.
相關臨床試驗
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相關器械（代碼：JKA）
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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