照護調度器
K 號：K181053 · 2019-01-04
廣告
器材摘要
Care Orchestrator is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 2019-01-04 under 510(k) number K181053. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Care Orchestrator?
Care Orchestrator is a medical device that received FDA 510(k) clearance on 2019-01-04. The listed applicant is Respironics, Inc.. The 510(k) number is K181053.
When did Care Orchestrator receive FDA 510(k) clearance?
Care Orchestrator received FDA 510(k) clearance on 2019-01-04, under 510(k) number K181053.
Who is the listed applicant for Care Orchestrator?
FDA 510(k) 記錄將Respironics, Inc.列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for Care Orchestrator?
The FDA product code for Care Orchestrator is BZD.
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 Respironics, 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。
相關器械（代碼：BZD）
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