內科手術VSP軟體設備
K 號：K213128 · 2022-10-21
廣告
器材摘要
IntraOp VSP Software Device is the device name listed in this FDA 510(k) record. The listed applicant is Xironetic, LLC. It received FDA 510(k) clearance on 2022-10-21 under 510(k) number K213128. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the IntraOp VSP Software Device?
IntraOp VSP Software Device is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Xironetic, LLC. The 510(k) number is K213128.
When did IntraOp VSP Software Device receive FDA 510(k) clearance?
IntraOp VSP Software Device received FDA 510(k) clearance on 2022-10-21, under 510(k) number K213128.
Who is the listed applicant for IntraOp VSP Software Device?
The FDA 510(k) record lists Xironetic, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IntraOp VSP Software Device?
The FDA product code for IntraOp VSP Software Device is LLZ.
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。
相關器械（代碼：LLZ）
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