Z-Robot 患者定位系統
K 號：K182683 · 2019-06-27
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器材摘要
Z-Robot Patient Positioning System is the device name listed in this FDA 510(k) record. The listed applicant is Chinan Biomedical Technology, Inc.. It received FDA 510(k) clearance on 2019-06-27 under 510(k) number K182683. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Z-Robot Patient Positioning System?
Z-Robot Patient Positioning System is a medical device that received FDA 510(k) clearance on 2019-06-27. The listed applicant is Chinan Biomedical Technology, Inc.. The 510(k) number is K182683.
When did Z-Robot Patient Positioning System receive FDA 510(k) clearance?
Z-Robot Patient Positioning System received FDA 510(k) clearance on 2019-06-27, under 510(k) number K182683.
Who is the listed applicant for Z-Robot Patient Positioning System?
The FDA 510(k) record lists Chinan Biomedical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Z-Robot Patient Positioning System?
The FDA product code for Z-Robot Patient Positioning System is JAI.
相關臨床試驗
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相關器械（代碼：JAI）
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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