CORIOGRAPH 預術規劃與建模服務
K 號：K242272 · 2024-11-15
廣告
器材摘要
CORIOGRAPH Pre-Op Planning and Modeling Services is the device name listed in this FDA 510(k) record. The listed applicant is Blue Belt Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-15 under 510(k) number K242272. FDA Decision: Substantially Equivalent.
常見問題
What is the CORIOGRAPH Pre-Op Planning and Modeling Services?
CORIOGRAPH Pre-Op Planning and Modeling Services is a medical device that received FDA 510(k) clearance on 2024-11-15. The listed applicant is Blue Belt Technologies, Inc.. The 510(k) number is K242272.
When did CORIOGRAPH Pre-Op Planning and Modeling Services receive FDA 510(k) clearance?
CORIOGRAPH Pre-Op Planning and Modeling Services received FDA 510(k) clearance on 2024-11-15, under 510(k) number K242272.
Who is the listed applicant for CORIOGRAPH Pre-Op Planning and Modeling Services?
The FDA 510(k) record lists Blue Belt Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
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。
其他以 Blue Belt Technologies, Inc. 為申請人之記錄
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