支架，解剖修復
PMA 核准號：P180034 · 2022-09-29
廣告
決定日期2022-09-29
PMA 編號P180034
產品代碼QCT
器械分類3 類
醫療專科U
諮詢委員會履歷
器材摘要
Scaffold, dissection repair is the device name listed in this FDA 510(k) record. The listed applicant is Philips Image Guided Therapy Corporation. It received FDA 510(k) clearance on 2022-09-29. The device is classified under product code QCT. It was reviewed by the CV advisory panel.
常見問題
What is the Scaffold, dissection repair?
Scaffold, dissection repair is a medical device that received FDA 510(k) clearance on 2022-09-29. The listed applicant is Philips Image Guided Therapy Corporation.
When did Scaffold, dissection repair receive FDA 510(k) clearance?
The clearance date for Scaffold, dissection repair can be found in the official FDA records.
Who is the listed applicant for Scaffold, dissection repair?
The FDA 510(k) record lists Philips Image Guided Therapy Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Scaffold, dissection repair?
The FDA product code for Scaffold, dissection repair is QCT.
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。
廣告