SENYINT 遠端諮詢系統
K 號：K162727 · 2018-02-08
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器材摘要
SENYINT Remote Consultation System is the device name listed in this FDA 510(k) record. The listed applicant is Dalian Senyint Digital Medical System Co., Ltd.. It received FDA 510(k) clearance on 2018-02-08 under 510(k) number K162727. 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 SENYINT Remote Consultation System?
SENYINT Remote Consultation System is a medical device that received FDA 510(k) clearance on 2018-02-08. The listed applicant is Dalian Senyint Digital Medical System Co., Ltd.. The 510(k) number is K162727.
When did SENYINT Remote Consultation System receive FDA 510(k) clearance?
SENYINT Remote Consultation System received FDA 510(k) clearance on 2018-02-08, under 510(k) number K162727.
Who is the listed applicant for SENYINT Remote Consultation System?
The FDA 510(k) record lists Dalian Senyint Digital Medical System Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENYINT Remote Consultation System?
The FDA product code for SENYINT Remote Consultation System is LLZ.
相關臨床試驗
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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。
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