MindsEye 可擴充端口
K 號：K202072 · 2020-08-26
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器材摘要
MindsEye Expandable Port is the device name listed in this FDA 510(k) record. The listed applicant is Minnetronix Neuro, Inc.. It received FDA 510(k) clearance on 2020-08-26 under 510(k) number K202072. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MindsEye Expandable Port?
MindsEye Expandable Port is a medical device that received FDA 510(k) clearance on 2020-08-26. The listed applicant is Minnetronix Neuro, Inc.. The 510(k) number is K202072.
When did MindsEye Expandable Port receive FDA 510(k) clearance?
MindsEye Expandable Port received FDA 510(k) clearance on 2020-08-26, under 510(k) number K202072.
Who is the listed applicant for MindsEye Expandable Port?
The FDA 510(k) record lists Minnetronix Neuro, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MindsEye Expandable Port?
The FDA product code for MindsEye Expandable Port is GZT.
相關臨床試驗
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相關器械（代碼：GZT）
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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