KIT, DNA偵測，人類乳突病毒
PMA 核准號：P080014 · 2018-11-15
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器材摘要
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS is the device name listed in this FDA 510(k) record. The listed applicant is Hologic, Inc.. It received FDA 510(k) clearance on 2018-11-15. The device is classified under product code MAQ. It was reviewed by the MI advisory panel.
常見問題
What is the KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS?
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS is a medical device that received FDA 510(k) clearance on 2018-11-15. The listed applicant is Hologic, Inc..
When did KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS receive FDA 510(k) clearance?
The clearance date for KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS can be found in the official FDA records.
誰是KIT，DNA偵測，人類乳頭病毒申請的列名申請人？
FDA 510(k) 記錄將霍洛基克公司（Hologic, Inc.）列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為KIT，DNA偵測，人類乳突病毒？
FDA產品代碼為KIT、DNA偵測、人類乳突病毒檢測的產品代碼為MAQ。
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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