處理器，子宮頸細胞涂片，自動化
PMA 核准號：P970018 · 2024-09-06
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器材摘要
Processor, cervical cytology slide, automated is the device name listed in this FDA 510(k) record. The listed applicant is Bd Diagnostic Systems. It received FDA 510(k) clearance on 2024-09-06. The device is classified under product code MKQ. It was reviewed by the PA advisory panel.
常見問題
What is the Processor, cervical cytology slide, automated?
Processor, cervical cytology slide, automated is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Bd Diagnostic Systems.
When did Processor, cervical cytology slide, automated receive FDA 510(k) clearance?
The clearance date for Processor, cervical cytology slide, automated can be found in the official FDA records.
Who is the listed applicant for Processor, cervical cytology slide, automated?
The FDA 510(k) record lists Bd Diagnostic Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Processor, cervical cytology slide, automated?
The FDA product code for Processor, cervical cytology slide, automated is MKQ.
相關臨床試驗
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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