MRI病人監護儀 TeslaDUO
K 號：K153739 · 2016-06-28
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器材摘要
MRI Patient Monitor TeslaDUO is the device name listed in this FDA 510(k) record. The listed applicant is Mipm Mammendorfer Institut Fur Physik Und Medizin. It received FDA 510(k) clearance on 2016-06-28 under 510(k) number K153739. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MRI Patient Monitor TeslaDUO?
MRI Patient Monitor TeslaDUO is a medical device that received FDA 510(k) clearance on 2016-06-28. The listed applicant is Mipm Mammendorfer Institut Fur Physik Und Medizin. The 510(k) number is K153739.
When did MRI Patient Monitor TeslaDUO receive FDA 510(k) clearance?
MRI Patient Monitor TeslaDUO received FDA 510(k) clearance on 2016-06-28, under 510(k) number K153739.
Who is the listed applicant for MRI Patient Monitor TeslaDUO?
The FDA 510(k) record lists Mipm Mammendorfer Institut Fur Physik Und Medizin as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRI Patient Monitor TeslaDUO?
The FDA product code for MRI Patient Monitor TeslaDUO is MWI.
相關臨床試驗
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相關器械（代碼：MWI）
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。
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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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